Multimorbidity_hearing loss

Metadata

Coding system
SNOMED CT (UK Clinical Edition)
Coding system release
40.4.0
Organisation
University of Bristol
Codelist ID
bristol/multimorbidity_hearing-loss
Version ID
6c165b67
Number of codes included
515

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Versions

  1. 6c165b67 Published
    Created: 09 Sep 2025 at 21:49

About

Description

Updated to include syndromes which include deafness

Methodology

Review by GP

Signed off by

  • Luisa Pettigrew, (July 15, 2025)
  • Mengxuan Zou, (July 15, 2025)

Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.

We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.

code term
1010229008 Neural hearing loss of left ear
1010230003 Neural hearing loss of right ear
1010236009 Conductive hearing loss of right ear
1010238005 Conductive hearing loss of left ear
1010439000 Conductive hearing loss of left ear with normal hearing on right side
1010440003 Conductive hearing loss of right ear with normal hearing on left side
1010441004 Sensorineural hearing loss of right ear with normal hearing on left side
1010442006 Sensorineural hearing loss of left ear with normal hearing on right side
1010606009 Waardenburg syndrome type 1
1010610007 Retinitis pigmentosa-deafness syndrome type 3
1010636000 Waardenburg syndrome type 2
10170007 Black locks, oculocutaneous albinism, AND deafness of the sensorineural type
103276001 Decreased hearing
103303007 Hearing loss remits during vertigo attacks
104121000000105 Low frequency deafness
1052205008 Mixed conductive and sensorineural hearing loss of left ear with normal hearing on right side
1052206009 Mixed conductive and sensorineural hearing loss of right ear with normal hearing on left side
1083811000119108 High frequency sensorineural hearing loss of bilateral ears
1084051000119104 Conductive hearing loss of bilateral middle ears
1084151000119100 Hearing loss of bilateral ears caused by noise
1089221000119100 Hearing loss of left ear caused by noise
10901651000119106 Injury of right acoustic nerve
10901691000119101 Injury of left acoustic nerve
1091831000119101 Hearing loss of right ear caused by noise
110271000000105 High frequency deafness
111339003 Congenital anomaly of ear with impairment of hearing
111543003 Partial deafness
1119386008 Sensorineural hearing loss of right ear
1119387004 Sensorineural hearing loss of left ear
1142112002 Sensorineural deafness due to late congenital syphilis
1167372000 X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome
1169356004 Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome
1172604004 Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome
1172605003 Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome
1172635005 Split-foot malformation, mesoaxial polydactyly syndrome
1173035001 Combined oxidative phosphorylation defect type 25
1179361001 Maternal perinatal sensorineural hearing loss
1179362008 Neonatal sensorineural hearing loss
1179555000 Fetal sensorineural hearing loss
118230007 Hearing finding
1187039001 Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome
1187512003 Non-syndromic mitochondrial sensorineural deafness
1197059004 Congenital ichthyosis, microcephalus, tetraplegia syndrome
1204415006 Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome
1208614008 Autosomal dominant deafness with onychodystrophy syndrome
1217379007 NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy
1220595008 Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
1222649004 Auditory neuropathy, optic atrophy syndrome
1222655009 Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome
1228871002 Proliferating cell nuclear antigen-related progressive neurodegenerative photosensitivity syndrome
1229999001 Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome
1230014007 Duane retraction syndrome with congenital deafness
1230412003 Profound hearing loss
1234911006 Congenital cochleovestibular malformation
1237343009 Otodental syndrome
1237413006 Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome
1254651003 Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome
1255271005 Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome
1260133007 Syndromic sensorineural deafness due to combined oxidative phosphorylation defect
1260199008 Non-syndromic genetic hearing loss
1260450002 Infantile multisystem neurologic, endocrine, pancreatic disease
1268415009 High frequency sensorineural hearing loss
1268429005 High frequency conductive hearing loss
1268466004 Low frequency sensorineural hearing loss
1268467008 Low frequency conductive hearing loss
1271009 Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome
1281843005 Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome
1284851009 Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome
1285518004 Wolfram syndrome type 1
1285519007 Wolfram syndrome type 2
129629004 Metabolic presbycusis
129630009 Mechanical presbycusis
129631008 Birth trauma deafness
1299152003 Adult-onset progressive leukoencephalopathy, early-onset deafness
1300194008 Mitchell syndrome
1332382002 Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome
1356736002 Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome
139613003 Deafness (& symptom)
141268007 O/E - High tone deafness
15123008 Familial amyloid nephropathy with urticaria AND deafness
151504001 Deafness remedial therapy
151507008 Deafness remedial therapy NOS
15188001 Hearing loss
15190000 Tympanic membrane conductive hearing loss
155242002 Other ear disorders &/or hearing loss
155246004 Noise-induced hearing loss
155247008 Unspecified sudden hearing loss
155254002 Hearing loss
155255001 Conductive hearing loss
155256000 Deafness: [sensorineural] or [nerve] or [perceptive - diagnos]
155257009 Mixed conductive and sensorineural hearing loss
155259007 Deafness NOS
15984431000119109 Impairment of hearing of right ear co-occurrent and due to congenital ear malformation
15984471000119107 Impairment of hearing of left ear co-occurrent and due to congenital ear malformation
15984511000119103 Impairment of hearing of bilateral ears co-occurrent and due to congenital ear malformation
162340000 Hearing difficulty
162341001 Deafness (& symptom)
162342008 Unilateral deafness
162343003 Partial deafness
162344009 Bilateral deafness
162594009 Suspected deafness
164060004 On examination - slightly deaf
164061000 On examination - significantly deaf
164062007 On examination - very deaf
164063002 On examination - completely deaf
164068006 On examination - tune fork=conductive deaf
164069003 On examination - tune fork=perceptive deaf
164070002 On examination - High tone deafness
183123004 Provide head worn hearing aid
183124005 Provide body worn hearing aid
183125006 Ear fitting hearing aid
183280009 Deafness remedial therapy
183281008 Lip-reading training
183282001 Finger-reading training
183283006 Deafness remedial therapy NOS
186570004 Rubella deafness
192426006 [X] Dissociative anaesthesia and sensory loss (& [psychogenic deafness])
192566007 [X] Receptive language disorder (& [congenit auditory imperception] or [development dysphasia, receptive] or [development Wernicke's aphasia] or [word deafness] or [development aphasia, receptive])
194391007 Unspecified sudden hearing loss
194398001 Impaired auditory discrimination
194411005 Hearing loss (& [deafness])
194412003 Unspecified conductive hearing loss
194413008 Conductive hearing loss due to disorder of external ear
194414002 Conductive hearing loss due to disorder of tympanic membrane
194415001 Conductive hearing loss due to disorder of middle ear
194416000 Conductive hearing loss due to disorder of inner ear
194417009 Conductive hearing loss, bilateral
194418004 Unilateral conductive hearing loss with unrestricted hearing on the contralateral side
194419007 Combined conductive hearing loss
194420001 Conductive hearing loss NOS
194421002 Sensorineural hearing loss (& [deafness: [high frequency] or [low frequency])
194422009 Unspecified perceptive hearing loss
194423004 Ototoxicity - deafness (& [drug])
194424005 Sensorineural hearing loss of bilateral ears
194425006 Unilateral sensorineural hearing loss with unrestricted hearing on the contralateral side
194426007 Combined perceptive hearing loss
194427003 Perceptive hearing loss NOS
194428008 Unilateral mixed conductive and sensorineural hearing loss with unrestricted hearing on the contralateral side
194429000 Mixed conductive and sensorineural hearing loss, bilateral
194431009 Other specified forms of hearing loss
194432002 Deafness: [chronic] or [NOS]
194699002 [X]Other specified hearing loss
197501000000104 Hearing disability
204224006 Ear anomalies with hearing impairment
204240009 (Other and unspecified ear anomaly with hearing impaired) or (deafness due to congenital anomaly NEC)
2061000 Conductive hearing loss of combined sites
212147006 (Nerve injury: [auditory cranial] or [eighth] or [acoustic (8th)]) or (traumatic deafness NOS)
21451000119101 Mild to moderate hearing loss
22181003 Diplacusis
229643008 Voice associated with deafness
229749000 Congenital auditory agnosia
232057003 Usher syndrome type 1
232058008 Usher syndrome type 2
232183005 Insertion of bone anchors for subcutaneous bone anchored hearing aid
232302007 Mondini defect
232325008 Chronic deafness
232326009 High frequency deafness
232327000 Low frequency deafness
232328005 Dominant sensorineural hearing loss
232329002 X-linked sensorineural hearing loss
232330007 Recessive sensorineural hearing loss
232331006 Perinatal sensorineural hearing loss
232332004 Postnatal acquired sensorineural hearing loss
232333009 Hearing loss associated with syndrome
236529001 Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness
236532003 Renal tubular acidosis with progressive nerve deafness
237612000 Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
237617006 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
237619009 Maternally inherited diabetes and deafness
237918004 Waardenburg syndrome type 3
238047006 Beta-D-mannosidosis
239010003 Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia
239059004 Keratitis ichthyosis and deafness syndrome
239061008 Keratosis pilaris with ichthyosis and deafness
240554006 Hutchinson's triad
242881000000103 Hearing lateralised to left
242891000000101 Hearing lateralised to right
247283005 Binaural diplacusis
2521009 Bone conduction better than air
253246000 Deafness due to congenital anomaly NEC
254173004 Hystrix ichthyosis with deafness
2625009 Senter syndrome
262764000 Noise-induced permanent threshold shift
26718008 Robinson nail dystrophy-deafness syndrome
267677007 Ototoxicity - deafness
267678002 Deafness NOS
267764005 Other ear disorders &/or hearing loss
267770004 Deafness: [sensorineural] or [nerve] or [perceptive - diagnos]
269042000 O/E - conductive deaf (&tune fork=)
269043005 O/E - perceptive deaf (&tune fork=)
272033007 Deafness symptom
274570008 [EDTA] Hereditary nephritis with nerve deafness (Alport's Syndrome) associated with renal failure
27472009 Weber's test, lateralized left
275482009 Drug ototoxicity - deafness
275879008 On examination - deaf
277214003 Sound lateralized to affected ear
277215002 Sound lateralized to non-affected ear
277216001 Sound perceived in midline
277424008 Postoperative profound sensorineural hearing loss
277431007 Monaural diplacusis
277433005 Difficulty hearing in noise
277663005 Simulated hearing loss
280122007 Hearing worse
281656009 Hearing aid provision
285055002 Does use hearing aid
290006 Melnick-Fraser syndrome
300210001 No response to sound
300223008 Hearing for conversational voice impaired
300225001 Hearing for loud voice impaired
300227009 Hearing for voice impaired
300228004 Hearing problem
30169000 Psychogenic deafness
306913003 Second stage bone anchored hearing aid procedure
306970008 Unable to hear whisper
306971007 Unable to hear conversational voice
306972000 Unable to hear loud voice
314914004 Deteriorating hearing
31732001 Weber's test, lateralized right
335601000000105 Maternally inherited deafness
338081000000101 Maternally inherited deafness
343087000 Partial deafness
3508009 Osteogenesis imperfecta with blue sclerae
3561000119106 Severe hearing loss
36543008 Echo diplacusis
366104009 Finding of lateralization of sound
368851000000106 Hearing loss
373905003 Jervell and Lange-Nielsen syndrome
37635004 Toxic deafness
3820005 Inner ear conductive hearing loss
390967001 Hearing aid problem
401008002 Difficulty hearing with background noise
401009005 Difficulty hearing whisper
401991000000109 [X] Receptive language disorder (& [congenit auditory imperception] or [development dysphasia, receptive] or [development Wernicke's aphasia] or [word deafness] or [development aphasia, receptive])
403780007 Autosomal recessive keratitis-ichthyosis-deafness syndrome
403791000 Keratoderma with deafness
403805009 Albinism-deafness syndrome of Tietz
40897007 Occupational deafness
411511000000107 [V]Fitting or adjustment of hearing aid
423303001 Difficulty hearing high frequency sounds
424723006 Difficulty hearing speech in large group setting
425091001 Difficulty hearing normal speech tones
42538001 Low frequency deafness
425601005 Unilateral neural hearing loss
425980006 Unilateral sensory hearing loss
427644005 Bilateral central hearing loss
427772009 Asymmetrical hearing loss
428470000 Autoimmune sensorineural hearing loss
42853003 Paradoxic hearing loss
428887009 Asymmetrical sensorineural hearing loss
430977001 Bilateral neural hearing loss
430985005 Bilateral sensory hearing loss
433147009 Combined visual and hearing impairment
43659006 Auditory agnosia
44057004 Conductive hearing loss
441719005 Speech and language developmental delay due to hearing loss
442535004 Unilateral conductive hearing loss
443511000000102 [X] Dissociative anaesthesia and sensory loss (& [psychogenic deafness])
443805006 Auditory neuropathy spectrum disorder
446499008 Provision of replacement hearing aid
447489005 Provision of replacement hearing aid component
46050004 Bone conduction deafness
466101000000106 [X]Other specified hearing loss
47111006 External ear conductive hearing loss
471391000000101 Hereditary nephritis with nerve deafness (Alport's Syndrome) associated with renal failure - European Dialysis and Transplant Association
473421004 Deafness of right ear
473422006 Deafness of left ear
473423001 Hearing loss of right ear
473424007 Hearing loss of left ear
47434006 Waardenburg syndrome
48436005 Articulatory defect due to conductive hearing loss
48758008 Upper frequency deafness
49526009 Presbycusis
514793471000119104 Usher syndrome type 1F
52171000 Ocular albinism-lentigines-deafness syndrome
525751000000102 Congenital prelingual deafness
525761000000104 Mild acquired hearing loss
525771000000106 Moderate acquired hearing loss
525781000000108 Severe acquired hearing loss
525791000000105 Profound acquired hearing loss
5349006 Weber's test, central
54036001 Oto-palato-digital syndrome, type I
551921000000106 Deafness remedial therapy NOS
56943007 End organ deafness
57838006 Retinitis pigmentosa-deafness syndrome
60700002 Sensorineural hearing loss
609125008 Acquired sensorineural hearing loss
61444009 Disharmonic diplacusis
61743004 Middle ear conductive hearing loss
61947007 Deaf mutism
63702009 Alstrom syndrome
637261000000105 Deafness due to congenital anomaly NEC
643761000000109 Unspecified sudden hearing loss
65680009 Sensorineural hearing loss of combined sites
657751000000104 Other specified forms of hearing loss
672091000000109 Unspecified conductive hearing loss
672101000000101 Perceptive hearing loss NOS
67817003 Pili torti-deafness syndrome
679391000000103 Deafness NOS
68467004 Central hearing loss
694191000000109 Unspecified perceptive hearing loss
694201000000106 Conductive hearing loss NOS
698614006 Acquired deaf mutism
698615007 Congenital deaf mutism
699238006 Congenital prelingual deafness
699316006 Myhre syndrome
699866005 Progressive bulbar palsy with sensorineural deafness
700112007 Bartter syndrome type 4
700448000 Epilepsy, ataxia, sensorineural deafness, and tubulopathy syndrome
700453005 Congenital sensorineural hearing loss
700454004 Profound sensorineural hearing loss
700489002 Sensorineural deafness and male infertility
702360007 Congenital deafness with labyrinthine aplasia, microtia and microdontia
702362004 Craniofacial deafness hand syndrome
702423009 Deafness-dystonia-optic neuronopathy syndrome
702441001 Fatal X-linked ataxia with deafness and loss of vision
70348004 Pendred's syndrome
706771000000109 Congenital prelingual deafness
706781000000106 Mild acquired hearing loss
706791000000108 Moderate acquired hearing loss
706801000000107 Severe acquired hearing loss
706811000000109 Profound acquired hearing loss
70694009 Wolfram syndrome
70967007 Dissociative deafness
71055004 Mid frequency deafness
711409002 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome
715239002 Sudden sensorineural hearing loss
715483009 Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss
715504003 Spastic paraparesis co-occurrent with deafness
715506001 Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome
715527006 Deafness and oligodontia syndrome
715529009 Progressive deafness with stapes fixation
715952000 Waardenburg Shah syndrome
716007007 Cleft palate and cleft lip with deafness and sacral lipoma syndrome
716112005 Microcephaly with deafness and intellectual disability syndrome
716170005 Deafness with cataract and skeletal anomaly syndrome
716192009 Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome
716238003 Deafness with epiphyseal dysplasia and short stature syndrome
716239006 Hearing loss and salivary gland insensitivity to aldosterone syndrome
716243005 Deafness with malformation of ear and facial palsy syndrome
716245003 Deafness craniofacial syndrome
717761005 Choroideremia with deafness and obesity syndrome
717766000 Alport syndrome autosomal dominant
717767009 Alport syndrome autosomal recessive
717768004 Alport syndrome X-linked
717791000 Bartter syndrome type 4a
717826009 Hereditary sensory and autonomic neuropathy with deafness and global delay
717909004 Bilateral microtia with deafness and cleft palate syndrome
717944002 Branchiogenic deafness syndrome
718574003 Cleft palate with coloboma of eye and deafness syndrome
718681002 Oro-facial digital syndrome type 11
718714006 Deafness and hypogonadism syndrome
718763005 Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome
718773007 Epithelio-exfoliative colitis and deafness syndrome
719102004 Congenital cataract with ataxia and deafness syndrome
719272007 Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome
719305006 Stapes ankylosis with broad thumb and toe syndrome
719689005 Multiple epiphyseal dysplasia Beighton type
719800009 Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome
719817002 X-linked spinocerebellar ataxia type 3
719838008 X-linked hereditary sensory and autonomic neuropathy with deafness
720506002 Deafness and myopia syndrome
720515009 Distal arthrogryposis type 6
720517001 Ataxia with deafness and intellectual disability syndrome
720518006 Athabaskan brainstem dysgenesis syndrome
720519003 Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome
720567008 Bosley Salih Alorainy syndrome
720601000 Camptodactyly and tall stature with scoliosis and hearing loss syndrome
720612000 Cardiospondylocarpofacial syndrome
720634003 Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome
720639008 Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome
720640005 Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome
720749004 Congenital hereditary endothelial dystrophy and perceptive deafness syndrome
720859009 Ehlers-Danlos syndrome kyphoscoliotic and deafness type
720955004 Fine Lubinsky syndrome
720957007 Deafness with skeletal dysplasia and lip granuloma syndrome
721084001 Deaf blind hypopigmentation syndrome Yemenite type
721085000 Deafness, enamel hypoplasia, nail defect syndrome
721086004 Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
721087008 Deafness and intellectual disability Martin Probst type syndrome
721089006 Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
721092005 Developmental malformation, deafness, dystonia syndrome
721207002 Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome
721221000 Hirschsprung disease with deafness and polydactyly syndrome
721294001 Acquired hearing loss
721584005 Johnson neuroectodermal syndrome
721973006 Lipodystrophy, intellectual disability, deafness syndrome
722019000 Oculootoradial syndrome
722035007 Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome
722054007 Ocular albinism with late-onset sensorineural deafness
722108000 Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome
722111004 Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome
722203001 Palmoplantar keratoderma with deafness syndrome
722213009 Severe X-linked intellectual disability Gustavson type
722285005 Albinism with deafness syndrome
722293005 Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
722378009 Congenital cataract with deafness and hypogonadism syndrome
722389002 Congenital hereditary facial paralysis with variable hearing loss syndrome
722449007 Gingival fibromatosis with progressive deafness syndrome
722453009 Cutaneous mastocytosis, short stature, hearing loss syndrome
722468005 Distal renal tubular acidosis co-occurrent with sensorineural deafness
722476007 Thickened earlobe with conductive deafness syndrome
723452007 Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
723497003 Peripheral neuropathy with sensorineural hearing impairment syndrome
723504000 Ramos Arroyo syndrome
723611008 Split hand, split foot malformation with sensorineural hearing loss syndrome
723721007 Sensorineural hearing loss, early graying, essential tremor syndrome
723993005 Sensorineural deafness with dilated cardiomyopathy syndrome
724001005 Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome
724092009 Nephrosis, deafness, urinary tract, digital malformation syndrome
724093004 Nephropathy, deafness, hyperparathyroidism syndrome
724173009 Maternally inherited cardiomyopathy and hearing loss syndrome
724280001 Hypospadias, hypertelorism, coloboma, deafness syndrome
724282009 Hypoparathyroidism, deafness, renal disease syndrome
724636005 Sudden idiopathic hearing loss
725137007 Neutropenia, monocytopenia, deafness syndrome
726106004 X-linked diffuse leiomyomatosis with Alport syndrome
726621009 Caudal appendage deafness syndrome
726669007 Central nervous system calcification, deafness, tubular acidosis, anemia syndrome
72964008 Traumatic deafness, non-occupational
73119000 Retinitis pigmentosa-deafness-ataxia syndrome
732248005 Coxoauricular syndrome
732951005 Mitochondrial myopathy, lactic acidosis, deafness syndrome
732953008 Ectodermal dysplasia and sensorineural deafness syndrome
733029008 Autosomal dominant spastic paraplegia type 29
733050004 Dysmorphism, short stature, deafness, disorder of sex development syndrome
733065003 Myoclonus, cerebellar ataxia, deafness syndrome
733069009 Deafness, vitiligo, achalasia syndrome
733071009 Deafness, small bowel diverticulosis, neuropathy syndrome
733089005 Spastic paraplegia, nephritis, deafness syndrome
73310008 Air conduction deafness
733419006 Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome
73371001 Neural hearing loss
734022008 Wolfram-like syndrome
73415002 Noise-induced hearing loss
737047001 Mild acquired hearing loss
737048006 Moderate acquired hearing loss
737049003 Severe acquired hearing loss
737050003 Profound acquired hearing loss
737344003 Congenital conductive hearing loss
737377004 Congenital mixed conductive and sensorineural hearing loss
74990005 Distorted hearing
761591000000105 Wears bone anchored hearing aid
763136000 Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
763213001 Conductive deafness, ptosis, skeletal anomalies syndrome
763279007 Facial dysmorphism, conductive hearing loss, heart defect syndrome
763688008 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome
763774001 Keipert syndrome
764097002 Postlingual non-syndromic genetic deafness
764098007 Prelingual non-syndromic genetic deafness
764810000 Branchiootic syndrome
765178008 Total visual and total hearing impairment
765325002 Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
766249007 Deafness, nephritis, anorectal malformation syndrome
766870005 Epiphyseal dysplasia, hearing loss, dysmorphism syndrome
770414008 Alport syndrome
770751003 Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome
770784003 Sinoatrial node dysfunction and deafness
770944002 Oculootodental syndrome
771308008 Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome
773398005 Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
773406003 Mandibular hypoplasia, deafness, progeroid syndrome
773575001 Ocular albinism with congenital sensorineural deafness
773583007 Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome
773610007 Chudley McCullough syndrome
773647007 Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome
773648002 Congenital cataract, hearing loss, severe developmental delay syndrome
773665006 Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome
773667003 Hypertelorism, preauricular sinus, punctual pits, deafness syndrome
773735007 Deafness with onychodystrophy syndrome
77507001 Mixed conductive AND sensorineural hearing loss
782690007 Gemignani syndrome
782752005 Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome
782942003 Renal caliceal diverticuli and deafness syndrome
783097004 Stickler syndrome type 3
783555001 Hypotrichosis and deafness syndrome
783614008 Familial steroid-resistant nephrotic syndrome with sensorineural deafness
783742004 Conductive hearing loss, malformation of external ear syndrome
788873009 Auditory synaptopathy
788953003 Hereditary hearing loss
79442007 Deafmutism-retinal degeneration syndrome
79471008 Sudden hearing loss
79665007 Wildervanck syndrome
80695003 Nerve conduction deafness
816067005 Diabetes, hypogonadism, deafness, intellectual disability syndrome
84063009 Traumatic deafness, occupational
8531006 Complete deafness
85571008 Sensory hearing loss
857091000000101 Renal tubular acidosis with progressive nerve deafness
857151000000105 Diabetes insipidus, diabetes mellitus, optic atrophy and deafness
860801000000109 Moderate sensorineural hearing loss
860811000000106 Severe sensorineural hearing loss
860841000000107 Profound sensorineural hearing loss
860851000000105 Mild sensorineural hearing loss
877191000000104 Bilateral profound sensorineural hearing loss
877201000000102 Bilateral profound sensorineural hearing loss
877211000000100 Bilateral congenital sensorineural hearing loss
877221000000106 Bilateral congenital sensorineural hearing loss
887101000000101 Epilepsy, ataxia, sensorineural deafness and tubulopathy syndrome
890361000000100 Profound sensorineural hearing loss
891381000000102 Moderate sensorineural hearing loss
891391000000100 Mild sensorineural hearing loss
891401000000102 Severe sensorineural hearing loss
89496002 Traumatic deafness
898061000000101 Bilateral severe sensorineural hearing loss
898071000000108 Bilateral moderate sensorineural hearing loss
898081000000105 Bilateral mild sensorineural hearing loss
93466004 Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
941941000000108 Articulatory defect due to conductive hearing loss
9441002 Injury of acoustic nerve
95819006 Unilateral hearing loss
95820000 Bilateral hearing loss
95821001 Neonatal hearing loss
95828007 Congenital deafness
965691000000103 Articulatory defect due to conductive hearing loss
99241000000103 Diabetes insipidus,diabetes mellitus, optic atrophy and deafness

This page shows the search terms that were used to build the codelist. Concepts that match the search terms, but which were excluded, are in faint grey.

Deafness

Included 369 out of 401 matching concepts.

Show matching concepts
  • (Developmental aphasia) or (word deafness) (192144006)
  • (Nerve injury: [auditory cranial] or [eighth] or [acoustic (8th)]) or (traumatic deafness NOS) (212147006)
  • (Other and unspecified ear anomaly with hearing impaired) or (deafness due to congenital anomaly NEC) (204240009)
  • 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome (711409002)
  • Acquired sensorineural hearing loss (609125008)
  • Adult-onset progressive leukoencephalopathy, early-onset deafness (1299152003)
  • Air conduction deafness (73310008)
  • Albinism with deafness syndrome (722285005)
  • Albinism-deafness syndrome of Tietz (403805009)
  • Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia (239010003)
  • Alport syndrome (770414008)
  • Alport syndrome X-linked (717768004)
  • Alport syndrome autosomal dominant (717766000)
  • Alport syndrome autosomal recessive (717767009)
  • Alstrom syndrome (63702009)
  • Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome (773583007)
  • Asymmetrical sensorineural hearing loss (428887009)
  • Ataxia with deafness and intellectual disability syndrome (720517001)
  • Athabaskan brainstem dysgenesis syndrome (720518006)
  • Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (720519003)
  • Auditory Impairment, Deafness, Partially Hearing Therapy Outcome Measure amplification use activity score (1854011000000100)
  • Auditory Impairment, Deafness, Partially Hearing Therapy Outcome Measure carer wellbeing score (1854021000000106)
  • Auditory Impairment, Deafness, Partially Hearing Therapy Outcome Measure communication activity score (1854001000000102)
  • Auditory Impairment, Deafness, Partially Hearing Therapy Outcome Measure impairment score (1853971000000108)
  • Auditory Impairment, Deafness, Partially Hearing Therapy Outcome Measure participation score (1853981000000105)
  • Auditory Impairment, Deafness, Partially Hearing Therapy Outcome Measure wellbeing score (1853991000000107)
  • Auditory agnosia (43659006)
  • Auditory discrimination aphasia (3387000)
  • Auditory neuropathy, optic atrophy syndrome (1222649004)
  • Auditory synaptopathy (788873009)
  • Autoimmune sensorineural hearing loss (428470000)
  • Autosomal dominant aplasia and myelodysplasia (778006008)
  • Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (722293005)
  • Autosomal dominant deafness with onychodystrophy syndrome (1208614008)
  • Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome (1229999001)
  • Autosomal dominant spastic paraplegia type 29 (733029008)
  • Autosomal recessive keratitis-ichthyosis-deafness syndrome (403780007)
  • Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (1204415006)
  • Bartter syndrome type 4 (700112007)
  • Bartter syndrome type 4a (717791000)
  • Bilateral central hearing loss (427644005)
  • Bilateral congenital sensorineural hearing loss (877211000000100)
  • Bilateral deafness (162344009)
  • Bilateral microtia with deafness and cleft palate syndrome (717909004)
  • Bilateral mild sensorineural hearing loss (898081000000105)
  • Bilateral moderate sensorineural hearing loss (898071000000108)
  • Bilateral neural hearing loss (430977001)
  • Bilateral profound sensorineural hearing loss (877191000000104)
  • Bilateral sensory hearing loss (430985005)
  • Bilateral severe sensorineural hearing loss (898061000000101)
  • Birth trauma deafness (129631008)
  • Black locks, oculocutaneous albinism, AND deafness of the sensorineural type (10170007)
  • Bone conduction deafness (46050004)
  • Bosley Salih Alorainy syndrome (720567008)
  • Branchiogenic deafness syndrome (717944002)
  • Branchiootic syndrome (764810000)
  • Camptodactyly and tall stature with scoliosis and hearing loss syndrome (720601000)
  • Cardiospondylocarpofacial syndrome (720612000)
  • Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome (1220595008)
  • Caudal appendage deafness syndrome (726621009)
  • Central hearing loss (68467004)
  • Central nervous system calcification, deafness, tubular acidosis, anemia syndrome (726669007)
  • Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome (720634003)
  • Charcot-Marie-Tooth disease type IE (715666007)
  • Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome (763136000)
  • Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (1281843005)
  • Choroideremia with deafness and obesity syndrome (717761005)
  • Chronic deafness (232325008)
  • Chudley McCullough syndrome (773610007)
  • Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome (1187039001)
  • Cleft palate and cleft lip with deafness and sacral lipoma syndrome (716007007)
  • Cleft palate with coloboma of eye and deafness syndrome (718574003)
  • Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (720639008)
  • Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome (1332382002)
  • Combined conductive hearing loss (194419007)
  • Combined oxidative phosphorylation defect type 25 (1173035001)
  • Combined perceptive hearing loss (194426007)
  • Complete deafness (8531006)
  • Conductive deafness, ptosis, skeletal anomalies syndrome (763213001)
  • Conductive hearing loss (44057004)
  • Conductive hearing loss due to disorder of external ear (194413008)
  • Conductive hearing loss due to disorder of inner ear (194416000)
  • Conductive hearing loss due to disorder of middle ear (194415001)
  • Conductive hearing loss due to disorder of tympanic membrane (194414002)
  • Conductive hearing loss of bilateral middle ears (1084051000119104)
  • Conductive hearing loss of combined sites (2061000)
  • Conductive hearing loss of left ear (1010238005)
  • Conductive hearing loss of left ear with normal hearing on right side (1010439000)
  • Conductive hearing loss of right ear (1010236009)
  • Conductive hearing loss of right ear with normal hearing on left side (1010440003)
  • Conductive hearing loss, bilateral (194417009)
  • Conductive hearing loss, malformation of external ear syndrome (783742004)
  • Congenital auditory agnosia (229749000)
  • Congenital cataract with ataxia and deafness syndrome (719102004)
  • Congenital cataract with deafness and hypogonadism syndrome (722378009)
  • Congenital cataract, hearing loss, severe developmental delay syndrome (773648002)
  • Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome (773398005)
  • Congenital cochleovestibular malformation (1234911006)
  • Congenital conductive hearing loss (737344003)
  • Congenital deafness (95828007)
  • Congenital deafness with labyrinthine aplasia, microtia and microdontia (702360007)
  • Congenital hereditary endothelial dystrophy and perceptive deafness syndrome (720749004)
  • Congenital hereditary facial paralysis with variable hearing loss syndrome (722389002)
  • Congenital ichthyosis, microcephalus, tetraplegia syndrome (1197059004)
  • Congenital mixed conductive and sensorineural hearing loss (737377004)
  • Congenital prelingual deafness (699238006)
  • Congenital prelingual deafness (525751000000102)
  • Congenital prelingual deafness (706771000000109)
  • Congenital sensorineural hearing loss (700453005)
  • Connective tissue disorder due to lysyl hydroxylase-3 deficiency (763318007)
  • Coxoauricular syndrome (732248005)
  • Craniofacial deafness hand syndrome (702362004)
  • Cutaneous mastocytosis, short stature, hearing loss syndrome (722453009)
  • Deaf blind hypopigmentation syndrome Yemenite type (721084001)
  • Deafness (& symptom) (162341001)
  • Deafness (& symptom) (139613003)
  • Deafness NOS (267678002)
  • Deafness NOS (679391000000103)
  • Deafness NOS (155259007)
  • Deafness and hypogonadism syndrome (718714006)
  • Deafness and intellectual disability Martin Probst type syndrome (721087008)
  • Deafness and myopia syndrome (720506002)
  • Deafness and oligodontia syndrome (715527006)
  • Deafness craniofacial syndrome (716245003)
  • Deafness due to congenital anomaly NEC (253246000)
  • Deafness due to congenital anomaly NEC (637261000000105)
  • Deafness of left ear (473422006)
  • Deafness of right ear (473421004)
  • Deafness remedial therapy (151504001)
  • Deafness remedial therapy (183280009)
  • Deafness remedial therapy NOS (551921000000106)
  • Deafness remedial therapy NOS (151507008)
  • Deafness remedial therapy NOS (183283006)
  • Deafness symptom (272033007)
  • Deafness with cataract and skeletal anomaly syndrome (716170005)
  • Deafness with epiphyseal dysplasia and short stature syndrome (716238003)
  • Deafness with malformation of ear and facial palsy syndrome (716243005)
  • Deafness with onychodystrophy syndrome (773735007)
  • Deafness with skeletal dysplasia and lip granuloma syndrome (720957007)
  • Deafness, enamel hypoplasia, nail defect syndrome (721085000)
  • Deafness, encephaloneuropathy, obesity, valvulopathy syndrome (763688008)
  • Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome (721086004)
  • Deafness, nephritis, anorectal malformation syndrome (766249007)
  • Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (719800009)
  • Deafness, small bowel diverticulosis, neuropathy syndrome (733071009)
  • Deafness, vitiligo, achalasia syndrome (733069009)
  • Deafness-dystonia-optic neuronopathy syndrome (702423009)
  • Deafness: [chronic] or [NOS] (194432002)
  • Deafness: [sensorineural] or [nerve] or [perceptive - diagnos] (155256000)
  • Deafness: [sensorineural] or [nerve] or [perceptive - diagnos] (267770004)
  • Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (721089006)
  • Developmental malformation, deafness, dystonia syndrome (721092005)
  • Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (857151000000105)
  • Diabetes insipidus,diabetes mellitus, optic atrophy and deafness (99241000000103)
  • Diabetes, hypogonadism, deafness, intellectual disability syndrome (816067005)
  • Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome (1172604004)
  • Dissociative deafness (70967007)
  • Distal arthrogryposis type 6 (720515009)
  • Distal renal tubular acidosis co-occurrent with sensorineural deafness (722468005)
  • Dominant sensorineural hearing loss (232328005)
  • Drug ototoxicity - deafness (275482009)
  • Duane retraction syndrome with congenital deafness (1230014007)
  • Dysmorphism, short stature, deafness, disorder of sex development syndrome (733050004)
  • Ear pit syndrome (232335002)
  • Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome (1169356004)
  • Ectodermal dysplasia and sensorineural deafness syndrome (732953008)
  • Ehlers-Danlos syndrome kyphoscoliotic and deafness type (720859009)
  • Emberger syndrome (700057001)
  • End organ deafness (56943007)
  • Epilepsy, ataxia, sensorineural deafness and tubulopathy syndrome (887101000000101)
  • Epilepsy, ataxia, sensorineural deafness, and tubulopathy syndrome (700448000)
  • Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (766870005)
  • Epithelio-exfoliative colitis and deafness syndrome (718773007)
  • External ear conductive hearing loss (47111006)
  • FH: Deafness (137750000)
  • Facial dysmorphism, conductive hearing loss, heart defect syndrome (763279007)
  • Familial amyloid nephropathy with urticaria AND deafness (15123008)
  • Familial steroid-resistant nephrotic syndrome with sensorineural deafness (783614008)
  • Family history: Deafness (160353007)
  • Fatal X-linked ataxia with deafness and loss of vision (702441001)
  • Fear of deafness (699391000)
  • Fetal sensorineural hearing loss (1179555000)
  • Fine Lubinsky syndrome (720955004)
  • Finger-reading training (183282001)
  • Gemignani syndrome (782690007)
  • Gingival fibromatosis with progressive deafness syndrome (722449007)
  • Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance (93466004)
  • Growth delay due to insulin-like growth factor type 1 deficiency (724385009)
  • Hearing loss (368851000000106)
  • Hearing loss (& [deafness]) (194411005)
  • Hearing loss and salivary gland insensitivity to aldosterone syndrome (716239006)
  • Hearing loss associated with syndrome (232333009)
  • Hereditary nephritis with nerve deafness (Alport's Syndrome) associated with renal failure - European Dialysis and Transplant Association (471391000000101)
  • Hereditary sensory and autonomic neuropathy with deafness and global delay (717826009)
  • High frequency conductive hearing loss (1268429005)
  • High frequency deafness (232326009)
  • High frequency deafness (110271000000105)
  • High frequency sensorineural hearing loss (1268415009)
  • High frequency sensorineural hearing loss of bilateral ears (1083811000119108)
  • Hirschsprung disease with deafness and polydactyly syndrome (721221000)
  • Hutchinson's triad (240554006)
  • Hypertelorism, preauricular sinus, punctual pits, deafness syndrome (773667003)
  • Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome (773665006)
  • Hypoparathyroidism, deafness, renal disease syndrome (724282009)
  • Hypospadias, hypertelorism, coloboma, deafness syndrome (724280001)
  • Hypotrichosis and deafness syndrome (783555001)
  • Hystrix ichthyosis with deafness (254173004)
  • Infantile multisystem neurologic, endocrine, pancreatic disease (1260450002)
  • Inner ear conductive hearing loss (3820005)
  • Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (722035007)
  • Jervell and Lange-Nielsen syndrome (373905003)
  • Johnson neuroectodermal syndrome (721584005)
  • Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome (1255271005)
  • Keipert syndrome (763774001)
  • Keratitis ichthyosis and deafness syndrome (239059004)
  • Keratoderma hereditarium mutilans with ichthyosis syndrome (717183001)
  • Keratoderma with deafness (403791000)
  • Keratosis pilaris with ichthyosis and deafness (239061008)
  • Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (1271009)
  • Lip-reading training (183281008)
  • Lipodystrophy, intellectual disability, deafness syndrome (721973006)
  • Low frequency conductive hearing loss (1268467008)
  • Low frequency deafness (42538001)
  • Low frequency deafness (232327000)
  • Low frequency deafness (104121000000105)
  • Low frequency sensorineural hearing loss (1268466004)
  • Mandibular hypoplasia, deafness, progeroid syndrome (773406003)
  • Maternal perinatal sensorineural hearing loss (1179361001)
  • Maternally inherited cardiomyopathy and hearing loss syndrome (724173009)
  • Maternally inherited deafness (338081000000101)
  • Maternally inherited deafness (335601000000105)
  • Maternally inherited diabetes and deafness (237619009)
  • Mechanical presbycusis (129630009)
  • Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (237617006)
  • Metabolic presbycusis (129629004)
  • Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome (733419006)
  • Microcephaly with deafness and intellectual disability syndrome (716112005)
  • Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (1254651003)
  • Mid frequency deafness (71055004)
  • Middle ear conductive hearing loss (61743004)
  • Mild sensorineural hearing loss (860851000000105)
  • Mitchell syndrome (1300194008)
  • Mitochondrial myopathy, lactic acidosis, deafness syndrome (732951005)
  • Mixed conductive AND sensorineural hearing loss (77507001)
  • Mixed conductive and sensorineural hearing loss of left ear with normal hearing on right side (1052205008)
  • Mixed conductive and sensorineural hearing loss of right ear with normal hearing on left side (1052206009)
  • Mixed conductive and sensorineural hearing loss, bilateral (194429000)
  • Moderate sensorineural hearing loss (860801000000109)
  • Mondini defect (232302007)
  • Multiple epiphyseal dysplasia Beighton type (719689005)
  • Mutilating keratoderma (24559001)
  • Myhre syndrome (699316006)
  • Myoclonus, cerebellar ataxia, deafness syndrome (733065003)
  • Neonatal sensorineural hearing loss (1179362008)
  • Nephropathy, deafness, hyperparathyroidism syndrome (724093004)
  • Nephrosis, deafness, urinary tract, digital malformation syndrome (724092009)
  • Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome (773647007)
  • Nerve conduction deafness (80695003)
  • Neural hearing loss (73371001)
  • Neural hearing loss of left ear (1010229008)
  • Neural hearing loss of right ear (1010230003)
  • Neutropenia, monocytopenia, deafness syndrome (725137007)
  • Noise-induced permanent threshold shift (262764000)
  • Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome (771308008)
  • Non-syndromic genetic hearing loss (1260199008)
  • Non-syndromic mitochondrial sensorineural deafness (1187512003)
  • O/E - High tone deafness (141268007)
  • O/E - conductive deaf (&tune fork=) (269042000)
  • O/E - perceptive deaf (&tune fork=) (269043005)
  • Occupational deafness (40897007)
  • Ocular albinism with congenital sensorineural deafness (773575001)
  • Ocular albinism with late-onset sensorineural deafness (722054007)
  • Ocular albinism-lentigines-deafness syndrome (52171000)
  • Oculootodental syndrome (770944002)
  • Oculootoradial syndrome (722019000)
  • Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss (715483009)
  • On examination - High tone deafness (164070002)
  • On examination - tune fork=conductive deaf (164068006)
  • On examination - tune fork=perceptive deaf (164069003)
  • Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (1222655009)
  • Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (722108000)
  • Osteogenesis imperfecta with blue sclerae (3508009)
  • Oto-palato-digital syndrome, type I (54036001)
  • Otodental syndrome (1237343009)
  • Ototoxicity - deafness (267677007)
  • Ototoxicity - deafness (& [drug]) (194423004)
  • Palmoplantar keratoderma with deafness syndrome (722203001)
  • Partial deafness (343087000)
  • Partial deafness (162343003)
  • Partial deafness (111543003)
  • Partial transitory deafness (878796005)
  • Pendred's syndrome (70348004)
  • Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (765325002)
  • Peripheral neuropathy with sensorineural hearing impairment syndrome (723497003)
  • Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (782752005)
  • Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome (715506001)
  • Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (237612000)
  • Pili torti-deafness syndrome (67817003)
  • Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (723452007)
  • Postlingual non-syndromic genetic deafness (764097002)
  • Postnatal acquired sensorineural hearing loss (232332004)
  • Postoperative profound sensorineural hearing loss (277424008)
  • Prelingual non-syndromic genetic deafness (764098007)
  • Presbycusis (49526009)
  • Profound sensorineural hearing loss (700454004)
  • Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome (1237413006)
  • Progressive bulbar palsy with sensorineural deafness (699866005)
  • Progressive deafness with stapes fixation (715529009)
  • Progressive hereditary glomerulonephritis without deafness (236419006)
  • Progressive recessive dystrophic epidermolysis bullosa (434002)
  • Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (719272007)
  • Proliferating cell nuclear antigen-related progressive neurodegenerative photosensitivity syndrome (1228871002)
  • Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness (236529001)
  • Psychogenic deafness (30169000)
  • Ramos Arroyo syndrome (723504000)
  • Recessive sensorineural hearing loss (232330007)
  • Renal caliceal diverticuli and deafness syndrome (782942003)
  • Renal tubular acidosis with progressive nerve deafness (236532003)
  • Renal tubular acidosis with progressive nerve deafness (857091000000101)
  • Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome (1172605003)
  • Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (724001005)
  • Retinitis pigmentosa-deafness syndrome (57838006)
  • Retinitis pigmentosa-deafness syndrome type 3 (1010610007)
  • Retinitis pigmentosa-deafness-ataxia syndrome (73119000)
  • Robinson nail dystrophy-deafness syndrome (26718008)
  • Rubella deafness (186570004)
  • Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (721207002)
  • Sensorineural deafness and male infertility (700489002)
  • Sensorineural deafness due to late congenital syphilis (1142112002)
  • Sensorineural deafness with dilated cardiomyopathy syndrome (723993005)
  • Sensorineural hearing loss (60700002)
  • Sensorineural hearing loss (& [deafness: [high frequency] or [low frequency]) (194421002)
  • Sensorineural hearing loss of bilateral ears (194424005)
  • Sensorineural hearing loss of combined sites (65680009)
  • Sensorineural hearing loss of left ear (1119387004)
  • Sensorineural hearing loss of left ear with normal hearing on right side (1010442006)
  • Sensorineural hearing loss of right ear (1119386008)
  • Sensorineural hearing loss of right ear with normal hearing on left side (1010441004)
  • Sensorineural hearing loss, early graying, essential tremor syndrome (723721007)
  • Sensory hearing loss (85571008)
  • Senter syndrome (2625009)
  • Severe X-linked intellectual disability Gustavson type (722213009)
  • Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome (770751003)
  • Severe sensorineural hearing loss (860811000000106)
  • Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome (716192009)
  • Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome (1284851009)
  • Simulated hearing loss (277663005)
  • Sinoatrial node dysfunction and deafness (770784003)
  • Spastic paraparesis co-occurrent with deafness (715504003)
  • Spastic paraplegia, nephritis, deafness syndrome (733089005)
  • Split hand, split foot malformation with sensorineural hearing loss syndrome (723611008)
  • Split-foot malformation, mesoaxial polydactyly syndrome (1172635005)
  • Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome (718763005)
  • Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome (1356736002)
  • Stapes ankylosis with broad thumb and toe syndrome (719305006)
  • Stickler syndrome type 3 (783097004)
  • Sudden sensorineural hearing loss (715239002)
  • Suspected deafness (139862001)
  • Suspected deafness (162594009)
  • Syndromic sensorineural deafness due to combined oxidative phosphorylation defect (1260133007)
  • Temtamy preaxial brachydactyly syndrome (777998000)
  • Thickened earlobe with conductive deafness syndrome (722476007)
  • Tone deafness (55647004)
  • Total transitory deafness (878797001)
  • Total visual and total hearing impairment (765178008)
  • Toxic deafness (37635004)
  • Transient ischemic deafness (194387002)
  • Transient ischemic deafness (9711000)
  • Transitory deafness (878795009)
  • Traumatic deafness (89496002)
  • Traumatic deafness, non-occupational (72964008)
  • Traumatic deafness, occupational (84063009)
  • Triphalangeal thumbs with onychodystrophy (239047003)
  • Tympanic membrane conductive hearing loss (15190000)
  • Unilateral deafness (162342008)
  • Upper frequency deafness (48758008)
  • Usher syndrome type 1 (232057003)
  • Usher syndrome type 1F (514793471000119104)
  • Usher syndrome type 2 (232058008)
  • Voice associated with deafness (229643008)
  • Waardenburg Shah syndrome (715952000)
  • Waardenburg syndrome (47434006)
  • Waardenburg syndrome type 1 (1010606009)
  • Waardenburg syndrome type 2 (1010636000)
  • Waardenburg syndrome type 3 (237918004)
  • Wildervanck syndrome (79665007)
  • Wolfram syndrome (70694009)
  • Wolfram syndrome type 1 (1285518004)
  • Wolfram syndrome type 2 (1285519007)
  • Wolfram-like syndrome (734022008)
  • X-linked diffuse leiomyomatosis with Alport syndrome (726106004)
  • X-linked hereditary sensory and autonomic neuropathy with deafness (719838008)
  • X-linked sensorineural hearing loss (232329002)
  • X-linked spinocerebellar ataxia type 3 (719817002)
  • [EDTA] Hereditary nephritis with nerve deafness (Alport's Syndrome) associated with renal failure (274570008)
  • [V]Family history of deafness or hearing loss (315846009)
  • [V]Family history of deafness or hearing loss (440641000000105)
  • [X] Dissociative anaesthesia and sensory loss (& [psychogenic deafness]) (443511000000102)
  • [X] Dissociative anaesthesia and sensory loss (& [psychogenic deafness]) (192426006)
  • [X] Receptive language disorder (& [congenit auditory imperception] or [development dysphasia, receptive] or [development Wernicke's aphasia] or [word deafness] or [development aphasia, receptive]) (401991000000109)
  • [X] Receptive language disorder (& [congenit auditory imperception] or [development dysphasia, receptive] or [development Wernicke's aphasia] or [word deafness] or [development aphasia, receptive]) (192566007)

hearing loss

Included 387 out of 421 matching concepts.

Show matching concepts
  • 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome (711409002)
  • Acquired deaf mutism (698614006)
  • Acquired hearing loss (721294001)
  • Acquired sensorineural hearing loss (609125008)
  • Adult-onset progressive leukoencephalopathy, early-onset deafness (1299152003)
  • Air conduction deafness (73310008)
  • Albinism with deafness syndrome (722285005)
  • Albinism-deafness syndrome of Tietz (403805009)
  • Alport syndrome (770414008)
  • Alport syndrome X-linked (717768004)
  • Alport syndrome autosomal dominant (717766000)
  • Alport syndrome autosomal recessive (717767009)
  • Alstrom syndrome (63702009)
  • Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome (773583007)
  • Articulatory defect due to conductive hearing loss (48436005)
  • Articulatory defect due to conductive hearing loss (965691000000103)
  • Articulatory defect due to conductive hearing loss (941941000000108)
  • Asymmetrical hearing loss (427772009)
  • Asymmetrical sensorineural hearing loss (428887009)
  • At increased risk of aminoglycoside-induced hearing loss due to mitochondrially encoded 12S ribosomal ribonucleic acid genotype (2365501000000102)
  • At normal risk of aminoglycoside-induced hearing loss based on mitochondrially encoded 12S ribosomal ribonucleic acid genotype (2365511000000100)
  • Ataxia with deafness and intellectual disability syndrome (720517001)
  • Athabaskan brainstem dysgenesis syndrome (720518006)
  • Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (720519003)
  • Auditory neuropathy, optic atrophy syndrome (1222649004)
  • Auditory synaptopathy (788873009)
  • Autoimmune sensorineural hearing loss (428470000)
  • Autosomal dominant aplasia and myelodysplasia (778006008)
  • Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (722293005)
  • Autosomal dominant deafness with onychodystrophy syndrome (1208614008)
  • Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome (1229999001)
  • Autosomal dominant spastic paraplegia type 29 (733029008)
  • Autosomal recessive keratitis-ichthyosis-deafness syndrome (403780007)
  • Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (1204415006)
  • Bartter syndrome type 4 (700112007)
  • Bartter syndrome type 4a (717791000)
  • Beta-D-mannosidosis (238047006)
  • Bilateral central hearing loss (427644005)
  • Bilateral congenital sensorineural hearing loss (877211000000100)
  • Bilateral congenital sensorineural hearing loss (877221000000106)
  • Bilateral deafness (162344009)
  • Bilateral hearing loss (95820000)
  • Bilateral microtia with deafness and cleft palate syndrome (717909004)
  • Bilateral mild sensorineural hearing loss (898081000000105)
  • Bilateral moderate sensorineural hearing loss (898071000000108)
  • Bilateral neural hearing loss (430977001)
  • Bilateral profound sensorineural hearing loss (877191000000104)
  • Bilateral profound sensorineural hearing loss (877201000000102)
  • Bilateral sensory hearing loss (430985005)
  • Bilateral severe sensorineural hearing loss (898061000000101)
  • Birth trauma deafness (129631008)
  • Black locks, oculocutaneous albinism, AND deafness of the sensorineural type (10170007)
  • Bone conduction deafness (46050004)
  • Bosley Salih Alorainy syndrome (720567008)
  • Branchiogenic deafness syndrome (717944002)
  • Branchiootic syndrome (764810000)
  • Camptodactyly and tall stature with scoliosis and hearing loss syndrome (720601000)
  • Cardiospondylocarpofacial syndrome (720612000)
  • Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome (1220595008)
  • Caudal appendage deafness syndrome (726621009)
  • Central hearing loss (68467004)
  • Central nervous system calcification, deafness, tubular acidosis, anemia syndrome (726669007)
  • Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome (720634003)
  • Charcot-Marie-Tooth disease type IE (715666007)
  • Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome (763136000)
  • Child health screening for hearing (300831000000100)
  • Children's hearing screening (204631000000103)
  • Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (1281843005)
  • Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome (720640005)
  • Choroideremia with deafness and obesity syndrome (717761005)
  • Chronic deafness (232325008)
  • Chudley McCullough syndrome (773610007)
  • Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome (1187039001)
  • Cleft palate and cleft lip with deafness and sacral lipoma syndrome (716007007)
  • Cleft palate with coloboma of eye and deafness syndrome (718574003)
  • Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (720639008)
  • Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome (1332382002)
  • Combined conductive hearing loss (194419007)
  • Combined oxidative phosphorylation defect type 25 (1173035001)
  • Combined perceptive hearing loss (194426007)
  • Combined visual and hearing impairment (433147009)
  • Complete deafness (8531006)
  • Conductive hearing loss (44057004)
  • Conductive hearing loss (155255001)
  • Conductive hearing loss NOS (194420001)
  • Conductive hearing loss NOS (694201000000106)
  • Conductive hearing loss due to disorder of external ear (194413008)
  • Conductive hearing loss due to disorder of inner ear (194416000)
  • Conductive hearing loss due to disorder of middle ear (194415001)
  • Conductive hearing loss due to disorder of tympanic membrane (194414002)
  • Conductive hearing loss of bilateral middle ears (1084051000119104)
  • Conductive hearing loss of combined sites (2061000)
  • Conductive hearing loss of left ear (1010238005)
  • Conductive hearing loss of left ear with normal hearing on right side (1010439000)
  • Conductive hearing loss of right ear (1010236009)
  • Conductive hearing loss of right ear with normal hearing on left side (1010440003)
  • Conductive hearing loss, bilateral (194417009)
  • Conductive hearing loss, malformation of external ear syndrome (783742004)
  • Congenital anomaly of ear with impairment of hearing (111339003)
  • Congenital cataract with ataxia and deafness syndrome (719102004)
  • Congenital cataract with deafness and hypogonadism syndrome (722378009)
  • Congenital cataract, hearing loss, severe developmental delay syndrome (773648002)
  • Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome (773398005)
  • Congenital cochleovestibular malformation (1234911006)
  • Congenital conductive hearing loss (737344003)
  • Congenital deaf mutism (698615007)
  • Congenital deafness (95828007)
  • Congenital deafness with labyrinthine aplasia, microtia and microdontia (702360007)
  • Congenital hereditary endothelial dystrophy and perceptive deafness syndrome (720749004)
  • Congenital hereditary facial paralysis with variable hearing loss syndrome (722389002)
  • Congenital ichthyosis, microcephalus, tetraplegia syndrome (1197059004)
  • Congenital mixed conductive and sensorineural hearing loss (737377004)
  • Congenital prelingual deafness (699238006)
  • Congenital sensorineural hearing loss (700453005)
  • Coxoauricular syndrome (732248005)
  • Craniofacial deafness hand syndrome (702362004)
  • Cutaneous mastocytosis, short stature, hearing loss syndrome (722453009)
  • Deaf blind hypopigmentation syndrome Yemenite type (721084001)
  • Deaf mutism (61947007)
  • Deafmutism-retinal degeneration syndrome (79442007)
  • Deafness and hypogonadism syndrome (718714006)
  • Deafness and intellectual disability Martin Probst type syndrome (721087008)
  • Deafness and myopia syndrome (720506002)
  • Deafness and oligodontia syndrome (715527006)
  • Deafness craniofacial syndrome (716245003)
  • Deafness of left ear (473422006)
  • Deafness of right ear (473421004)
  • Deafness with cataract and skeletal anomaly syndrome (716170005)
  • Deafness with epiphyseal dysplasia and short stature syndrome (716238003)
  • Deafness with malformation of ear and facial palsy syndrome (716243005)
  • Deafness with onychodystrophy syndrome (773735007)
  • Deafness with skeletal dysplasia and lip granuloma syndrome (720957007)
  • Deafness, enamel hypoplasia, nail defect syndrome (721085000)
  • Deafness, encephaloneuropathy, obesity, valvulopathy syndrome (763688008)
  • Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome (721086004)
  • Deafness, nephritis, anorectal malformation syndrome (766249007)
  • Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (719800009)
  • Deafness, small bowel diverticulosis, neuropathy syndrome (733071009)
  • Deafness, vitiligo, achalasia syndrome (733069009)
  • Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (721089006)
  • Developmental malformation, deafness, dystonia syndrome (721092005)
  • Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome (1172604004)
  • Dissociative deafness (70967007)
  • Distal arthrogryposis type 6 (720515009)
  • Distal renal tubular acidosis co-occurrent with sensorineural deafness (722468005)
  • Dominant sensorineural hearing loss (232328005)
  • Drug ototoxicity - deafness (275482009)
  • Duane retraction syndrome with congenital deafness (1230014007)
  • Dysmorphism, short stature, deafness, disorder of sex development syndrome (733050004)
  • Ear pit syndrome (232335002)
  • Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome (1169356004)
  • Ectodermal dysplasia and sensorineural deafness syndrome (732953008)
  • Ehlers-Danlos syndrome kyphoscoliotic and deafness type (720859009)
  • End organ deafness (56943007)
  • Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (766870005)
  • External ear conductive hearing loss (47111006)
  • Facial dysmorphism, conductive hearing loss, heart defect syndrome (763279007)
  • Familial amyloid nephropathy with urticaria AND deafness (15123008)
  • Familial steroid-resistant nephrotic syndrome with sensorineural deafness (783614008)
  • Family history of hearing loss (439750006)
  • Family history of hearing loss (775691000000100)
  • Family history: Deafness (160353007)
  • Family history: Father deaf (160437008)
  • Fatal X-linked ataxia with deafness and loss of vision (702441001)
  • Fetal sensorineural hearing loss (1179555000)
  • Fine Lubinsky syndrome (720955004)
  • Gemignani syndrome (782690007)
  • Gingival fibromatosis with progressive deafness syndrome (722449007)
  • Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance (93466004)
  • Health and Safety Executive Categorisation Scheme - category Unilateral hearing loss (1107171000000101)
  • Hearing loss (15188001)
  • Hearing loss (155254002)
  • Hearing loss (368851000000106)
  • Hearing loss (& [deafness]) (194411005)
  • Hearing loss and salivary gland insensitivity to aldosterone syndrome (716239006)
  • Hearing loss associated with syndrome (232333009)
  • Hearing loss of bilateral ears caused by noise (1084151000119100)
  • Hearing loss of left ear (473424007)
  • Hearing loss of left ear caused by noise (1089221000119100)
  • Hearing loss of right ear (473423001)
  • Hearing loss of right ear caused by noise (1091831000119101)
  • Hearing loss remits during vertigo attacks (103303007)
  • Hereditary hearing loss (788953003)
  • Hereditary sensory and autonomic neuropathy with deafness and global delay (717826009)
  • High frequency conductive hearing loss (1268429005)
  • High frequency sensorineural hearing loss (1268415009)
  • High frequency sensorineural hearing loss of bilateral ears (1083811000119108)
  • Hirschsprung disease with deafness and polydactyly syndrome (721221000)
  • History of hearing loss (472955004)
  • Hutchinson's triad (240554006)
  • Hypertelorism, preauricular sinus, punctual pits, deafness syndrome (773667003)
  • Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome (773665006)
  • Hypoparathyroidism, deafness, renal disease syndrome (724282009)
  • Hypotrichosis and deafness syndrome (783555001)
  • Impairment of hearing of bilateral ears co-occurrent and due to congenital ear malformation (15984511000119103)
  • Impairment of hearing of left ear co-occurrent and due to congenital ear malformation (15984471000119107)
  • Impairment of hearing of right ear co-occurrent and due to congenital ear malformation (15984431000119109)
  • Infantile multisystem neurologic, endocrine, pancreatic disease (1260450002)
  • Inner ear conductive hearing loss (3820005)
  • Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (722035007)
  • Jervell and Lange-Nielsen syndrome (373905003)
  • Johnson neuroectodermal syndrome (721584005)
  • Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome (1255271005)
  • Keipert syndrome (763774001)
  • Keratitis ichthyosis and deafness syndrome (239059004)
  • Keratoderma hereditarium mutilans with ichthyosis syndrome (717183001)
  • Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (1271009)
  • Lipodystrophy, intellectual disability, deafness syndrome (721973006)
  • Low frequency conductive hearing loss (1268467008)
  • Low frequency sensorineural hearing loss (1268466004)
  • Mandibular hypoplasia, deafness, progeroid syndrome (773406003)
  • Maternal perinatal sensorineural hearing loss (1179361001)
  • Maternally inherited cardiomyopathy and hearing loss syndrome (724173009)
  • Maternally inherited diabetes and deafness (237619009)
  • Mechanical presbycusis (129630009)
  • Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (237617006)
  • Melnick-Fraser syndrome (290006)
  • Metabolic presbycusis (129629004)
  • Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome (733419006)
  • Microcephaly with deafness and intellectual disability syndrome (716112005)
  • Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (1254651003)
  • Mid frequency deafness (71055004)
  • Middle ear conductive hearing loss (61743004)
  • Mild acquired hearing loss (737047001)
  • Mild acquired hearing loss (525761000000104)
  • Mild acquired hearing loss (706781000000106)
  • Mild sensorineural hearing loss (860851000000105)
  • Mild sensorineural hearing loss (891391000000100)
  • Mild to moderate hearing loss (21451000119101)
  • Mitchell syndrome (1300194008)
  • Mitochondrial myopathy, lactic acidosis, deafness syndrome (732951005)
  • Mixed conductive AND sensorineural hearing loss (77507001)
  • Mixed conductive and sensorineural hearing loss (155257009)
  • Mixed conductive and sensorineural hearing loss of left ear with normal hearing on right side (1052205008)
  • Mixed conductive and sensorineural hearing loss of right ear with normal hearing on left side (1052206009)
  • Mixed conductive and sensorineural hearing loss, bilateral (194429000)
  • Moderate acquired hearing loss (737048006)
  • Moderate acquired hearing loss (706791000000108)
  • Moderate acquired hearing loss (525771000000106)
  • Moderate sensorineural hearing loss (860801000000109)
  • Moderate sensorineural hearing loss (891381000000102)
  • Mondini defect (232302007)
  • Multiple epiphyseal dysplasia Beighton type (719689005)
  • Mutilating keratoderma (24559001)
  • Myhre syndrome (699316006)
  • Myoclonus, cerebellar ataxia, deafness syndrome (733065003)
  • Neonatal hearing loss (95821001)
  • Neonatal sensorineural hearing loss (1179362008)
  • Nephropathy, deafness, hyperparathyroidism syndrome (724093004)
  • Nephrosis, deafness, urinary tract, digital malformation syndrome (724092009)
  • Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome (773647007)
  • Neural hearing loss (73371001)
  • Neural hearing loss of left ear (1010229008)
  • Neural hearing loss of right ear (1010230003)
  • Neutropenia, monocytopenia, deafness syndrome (725137007)
  • No family history of hearing loss (777581000000106)
  • No history of hearing loss (784061000000109)
  • No history of hearing loss (473073005)
  • Noise-induced hearing loss (73415002)
  • Noise-induced hearing loss (155246004)
  • Noise-induced permanent threshold shift (262764000)
  • Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome (771308008)
  • Non-syndromic genetic hearing loss (1260199008)
  • Non-syndromic mitochondrial sensorineural deafness (1187512003)
  • Occupational deafness (40897007)
  • Ocular albinism with late-onset sensorineural deafness (722054007)
  • Oculootodental syndrome (770944002)
  • Oculootoradial syndrome (722019000)
  • Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss (715483009)
  • Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (1222655009)
  • Oro-facial digital syndrome type 11 (718681002)
  • Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome (722111004)
  • Other ear disorders &/or hearing loss (267764005)
  • Other ear disorders &/or hearing loss (155242002)
  • Other specified forms of hearing loss (194431009)
  • Other specified forms of hearing loss (657751000000104)
  • Oto-palato-digital syndrome, type I (54036001)
  • Otodental syndrome (1237343009)
  • Ototoxicity - deafness (267677007)
  • Palmoplantar keratoderma with deafness syndrome (722203001)
  • Paradoxic hearing loss (42853003)
  • Partial deafness (343087000)
  • Partial transitory deafness (878796005)
  • Pattern of hearing loss (246459007)
  • Pendred's syndrome (70348004)
  • Perception of hearing loss (14230001000004101)
  • Perceptive hearing loss NOS (672101000000101)
  • Perceptive hearing loss NOS (194427003)
  • Perinatal sensorineural hearing loss (232331006)
  • Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (765325002)
  • Peripheral neuropathy with sensorineural hearing impairment syndrome (723497003)
  • Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (782752005)
  • Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome (715506001)
  • Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (237612000)
  • Pili torti-deafness syndrome (67817003)
  • Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (723452007)
  • Postlingual non-syndromic genetic deafness (764097002)
  • Postnatal acquired sensorineural hearing loss (232332004)
  • Postoperative profound sensorineural hearing loss (277424008)
  • Prelingual non-syndromic genetic deafness (764098007)
  • Presbycusis (49526009)
  • Profound acquired hearing loss (737050003)
  • Profound acquired hearing loss (525791000000105)
  • Profound acquired hearing loss (706811000000109)
  • Profound hearing loss (1230412003)
  • Profound sensorineural hearing loss (700454004)
  • Profound sensorineural hearing loss (860841000000107)
  • Profound sensorineural hearing loss (890361000000100)
  • Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome (1237413006)
  • Progressive bulbar palsy with sensorineural deafness (699866005)
  • Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (719272007)
  • Proliferating cell nuclear antigen-related progressive neurodegenerative photosensitivity syndrome (1228871002)
  • Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness (236529001)
  • Psychogenic deafness (30169000)
  • Ramos Arroyo syndrome (723504000)
  • Recessive sensorineural hearing loss (232330007)
  • Renal caliceal diverticuli and deafness syndrome (782942003)
  • Renal tubular acidosis with progressive nerve deafness (236532003)
  • Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome (1172605003)
  • Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (724001005)
  • Retinitis pigmentosa-deafness syndrome (57838006)
  • Retinitis pigmentosa-deafness syndrome type 3 (1010610007)
  • Retinitis pigmentosa-deafness-ataxia syndrome (73119000)
  • Robinson nail dystrophy-deafness syndrome (26718008)
  • Rubella deafness (186570004)
  • School entrant hearing screening (345401000000106)
  • Screening for hearing loss (710076008)
  • Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (721207002)
  • Sensorineural deafness and male infertility (700489002)
  • Sensorineural deafness due to late congenital syphilis (1142112002)
  • Sensorineural deafness with dilated cardiomyopathy syndrome (723993005)
  • Sensorineural hearing loss (60700002)
  • Sensorineural hearing loss (& [deafness: [high frequency] or [low frequency]) (194421002)
  • Sensorineural hearing loss of bilateral ears (194424005)
  • Sensorineural hearing loss of combined sites (65680009)
  • Sensorineural hearing loss of left ear (1119387004)
  • Sensorineural hearing loss of left ear with normal hearing on right side (1010442006)
  • Sensorineural hearing loss of right ear (1119386008)
  • Sensorineural hearing loss of right ear with normal hearing on left side (1010441004)
  • Sensorineural hearing loss, early graying, essential tremor syndrome (723721007)
  • Sensory hearing loss (85571008)
  • Senter syndrome (2625009)
  • Severe X-linked intellectual disability Gustavson type (722213009)
  • Severe acquired hearing loss (737049003)
  • Severe acquired hearing loss (706801000000107)
  • Severe acquired hearing loss (525781000000108)
  • Severe hearing loss (3561000119106)
  • Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome (770751003)
  • Severe sensorineural hearing loss (860811000000106)
  • Severe sensorineural hearing loss (891401000000102)
  • Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome (716192009)
  • Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome (1284851009)
  • Simulated hearing loss (277663005)
  • Sinoatrial node dysfunction and deafness (770784003)
  • Spastic paraparesis co-occurrent with deafness (715504003)
  • Spastic paraplegia, nephritis, deafness syndrome (733089005)
  • Special audiologic evaluation for functional hearing loss (91515000)
  • Speech and language developmental delay due to hearing loss (441719005)
  • Split hand, split foot malformation with sensorineural hearing loss syndrome (723611008)
  • Split-foot malformation, mesoaxial polydactyly syndrome (1172635005)
  • Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome (718763005)
  • Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome (1356736002)
  • Stapes ankylosis with broad thumb and toe syndrome (719305006)
  • Stickler syndrome type 3 (783097004)
  • Sudden hearing loss (79471008)
  • Sudden idiopathic hearing loss (724636005)
  • Sudden sensorineural hearing loss (715239002)
  • Syndromic sensorineural deafness due to combined oxidative phosphorylation defect (1260133007)
  • Temporary auditory threshold shift (1092791000119103)
  • Temporary auditory threshold shift of left ear (1089671000119102)
  • Temporary auditory threshold shift of right ear (1092281000119109)
  • Temtamy preaxial brachydactyly syndrome (777998000)
  • Thickened earlobe with conductive deafness syndrome (722476007)
  • Tone deafness (55647004)
  • Total transitory deafness (878797001)
  • Total visual and total hearing impairment (765178008)
  • Toxic deafness (37635004)
  • Transient ischemic deafness (194387002)
  • Transitory deafness (878795009)
  • Traumatic deafness (89496002)
  • Traumatic deafness, non-occupational (72964008)
  • Traumatic deafness, occupational (84063009)
  • Tympanic membrane conductive hearing loss (15190000)
  • Unilateral conductive hearing loss (442535004)
  • Unilateral conductive hearing loss with unrestricted hearing on the contralateral side (194418004)
  • Unilateral hearing loss (95819006)
  • Unilateral mixed conductive and sensorineural hearing loss with unrestricted hearing on the contralateral side (194428008)
  • Unilateral neural hearing loss (425601005)
  • Unilateral sensorineural hearing loss with unrestricted hearing on the contralateral side (194425006)
  • Unilateral sensory hearing loss (425980006)
  • Unspecified conductive hearing loss (194412003)
  • Unspecified conductive hearing loss (672091000000109)
  • Unspecified perceptive hearing loss (194422009)
  • Unspecified perceptive hearing loss (694191000000109)
  • Unspecified sudden hearing loss (155247008)
  • Unspecified sudden hearing loss (643761000000109)
  • Unspecified sudden hearing loss (194391007)
  • Upper frequency deafness (48758008)
  • Usher syndrome type 1 (232057003)
  • Usher syndrome type 1F (514793471000119104)
  • Usher syndrome type 2 (232058008)
  • Voice associated with deafness (229643008)
  • Waardenburg Shah syndrome (715952000)
  • Waardenburg syndrome (47434006)
  • Waardenburg syndrome type 1 (1010606009)
  • Waardenburg syndrome type 2 (1010636000)
  • Waardenburg syndrome type 3 (237918004)
  • Wildervanck syndrome (79665007)
  • Wolfram syndrome (70694009)
  • Wolfram syndrome type 1 (1285518004)
  • Wolfram syndrome type 2 (1285519007)
  • Wolfram-like syndrome (734022008)
  • X-linked diffuse leiomyomatosis with Alport syndrome (726106004)
  • X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome (1167372000)
  • X-linked hereditary sensory and autonomic neuropathy with deafness (719838008)
  • X-linked sensorineural hearing loss (232329002)
  • X-linked spinocerebellar ataxia type 3 (719817002)
  • [V]Family history of deafness or hearing loss (315846009)
  • [V]Family history of deafness or hearing loss (440641000000105)
  • [X]Other specified hearing loss (194699002)
  • [X]Other specified hearing loss (466101000000106)

sensorineural hearing loss

Included 201 out of 205 matching concepts.

Show matching concepts
  • 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome (711409002)
  • Acquired sensorineural hearing loss (609125008)
  • Adult-onset progressive leukoencephalopathy, early-onset deafness (1299152003)
  • Albinism with deafness syndrome (722285005)
  • Albinism-deafness syndrome of Tietz (403805009)
  • Alport syndrome (770414008)
  • Alport syndrome X-linked (717768004)
  • Alport syndrome autosomal dominant (717766000)
  • Alport syndrome autosomal recessive (717767009)
  • Alstrom syndrome (63702009)
  • Asymmetrical sensorineural hearing loss (428887009)
  • Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (720519003)
  • Auditory synaptopathy (788873009)
  • Autoimmune sensorineural hearing loss (428470000)
  • Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (722293005)
  • Autosomal dominant deafness with onychodystrophy syndrome (1208614008)
  • Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome (1229999001)
  • Autosomal dominant spastic paraplegia type 29 (733029008)
  • Bartter syndrome type 4 (700112007)
  • Bartter syndrome type 4a (717791000)
  • Bilateral central hearing loss (427644005)
  • Bilateral congenital sensorineural hearing loss (877211000000100)
  • Bilateral congenital sensorineural hearing loss (877221000000106)
  • Bilateral mild sensorineural hearing loss (898081000000105)
  • Bilateral moderate sensorineural hearing loss (898071000000108)
  • Bilateral neural hearing loss (430977001)
  • Bilateral profound sensorineural hearing loss (877191000000104)
  • Bilateral profound sensorineural hearing loss (877201000000102)
  • Bilateral sensory hearing loss (430985005)
  • Bilateral severe sensorineural hearing loss (898061000000101)
  • Black locks, oculocutaneous albinism, AND deafness of the sensorineural type (10170007)
  • Bosley Salih Alorainy syndrome (720567008)
  • Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome (1220595008)
  • Central hearing loss (68467004)
  • Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome (720634003)
  • Charcot-Marie-Tooth disease type IE (715666007)
  • Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome (763136000)
  • Choroideremia with deafness and obesity syndrome (717761005)
  • Chudley McCullough syndrome (773610007)
  • Cleft palate and cleft lip with deafness and sacral lipoma syndrome (716007007)
  • Cleft palate with coloboma of eye and deafness syndrome (718574003)
  • Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome (1332382002)
  • Combined oxidative phosphorylation defect type 25 (1173035001)
  • Combined perceptive hearing loss (194426007)
  • Congenital cataract with ataxia and deafness syndrome (719102004)
  • Congenital cataract with deafness and hypogonadism syndrome (722378009)
  • Congenital cataract, hearing loss, severe developmental delay syndrome (773648002)
  • Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome (773398005)
  • Congenital cochleovestibular malformation (1234911006)
  • Congenital hereditary endothelial dystrophy and perceptive deafness syndrome (720749004)
  • Congenital hereditary facial paralysis with variable hearing loss syndrome (722389002)
  • Congenital ichthyosis, microcephalus, tetraplegia syndrome (1197059004)
  • Congenital mixed conductive and sensorineural hearing loss (737377004)
  • Congenital sensorineural hearing loss (700453005)
  • Craniofacial deafness hand syndrome (702362004)
  • Deafness and intellectual disability Martin Probst type syndrome (721087008)
  • Deafness and oligodontia syndrome (715527006)
  • Deafness with cataract and skeletal anomaly syndrome (716170005)
  • Deafness with epiphyseal dysplasia and short stature syndrome (716238003)
  • Deafness with onychodystrophy syndrome (773735007)
  • Deafness with skeletal dysplasia and lip granuloma syndrome (720957007)
  • Deafness, enamel hypoplasia, nail defect syndrome (721085000)
  • Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome (721086004)
  • Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (719800009)
  • Deafness, small bowel diverticulosis, neuropathy syndrome (733071009)
  • Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (721089006)
  • Developmental malformation, deafness, dystonia syndrome (721092005)
  • Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome (1172604004)
  • Distal arthrogryposis type 6 (720515009)
  • Distal renal tubular acidosis co-occurrent with sensorineural deafness (722468005)
  • Dominant sensorineural hearing loss (232328005)
  • Drug ototoxicity - deafness (275482009)
  • Ectodermal dysplasia and sensorineural deafness syndrome (732953008)
  • Ehlers-Danlos syndrome kyphoscoliotic and deafness type (720859009)
  • End organ deafness (56943007)
  • Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (766870005)
  • Familial amyloid nephropathy with urticaria AND deafness (15123008)
  • Familial steroid-resistant nephrotic syndrome with sensorineural deafness (783614008)
  • Fetal sensorineural hearing loss (1179555000)
  • Gemignani syndrome (782690007)
  • Gingival fibromatosis with progressive deafness syndrome (722449007)
  • Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance (93466004)
  • Hearing loss and salivary gland insensitivity to aldosterone syndrome (716239006)
  • Hereditary sensory and autonomic neuropathy with deafness and global delay (717826009)
  • High frequency sensorineural hearing loss (1268415009)
  • High frequency sensorineural hearing loss of bilateral ears (1083811000119108)
  • Hutchinson's triad (240554006)
  • Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome (773665006)
  • Hypoparathyroidism, deafness, renal disease syndrome (724282009)
  • Hypotrichosis and deafness syndrome (783555001)
  • Infantile multisystem neurologic, endocrine, pancreatic disease (1260450002)
  • Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (722035007)
  • Jervell and Lange-Nielsen syndrome (373905003)
  • Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome (1255271005)
  • Keipert syndrome (763774001)
  • Keratoderma hereditarium mutilans with ichthyosis syndrome (717183001)
  • Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (1271009)
  • Lipodystrophy, intellectual disability, deafness syndrome (721973006)
  • Low frequency sensorineural hearing loss (1268466004)
  • Mandibular hypoplasia, deafness, progeroid syndrome (773406003)
  • Maternal perinatal sensorineural hearing loss (1179361001)
  • Maternally inherited cardiomyopathy and hearing loss syndrome (724173009)
  • Maternally inherited diabetes and deafness (237619009)
  • Mechanical presbycusis (129630009)
  • Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (237617006)
  • Metabolic presbycusis (129629004)
  • Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (1254651003)
  • Mid frequency deafness (71055004)
  • Mild sensorineural hearing loss (860851000000105)
  • Mild sensorineural hearing loss (891391000000100)
  • Mitochondrial myopathy, lactic acidosis, deafness syndrome (732951005)
  • Mixed conductive AND sensorineural hearing loss (77507001)
  • Mixed conductive and sensorineural hearing loss (155257009)
  • Mixed conductive and sensorineural hearing loss of left ear with normal hearing on right side (1052205008)
  • Mixed conductive and sensorineural hearing loss of right ear with normal hearing on left side (1052206009)
  • Mixed conductive and sensorineural hearing loss, bilateral (194429000)
  • Moderate sensorineural hearing loss (860801000000109)
  • Moderate sensorineural hearing loss (891381000000102)
  • Mondini defect (232302007)
  • Mutilating keratoderma (24559001)
  • Myhre syndrome (699316006)
  • Myoclonus, cerebellar ataxia, deafness syndrome (733065003)
  • Neonatal sensorineural hearing loss (1179362008)
  • Nephropathy, deafness, hyperparathyroidism syndrome (724093004)
  • Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome (773647007)
  • Neural hearing loss (73371001)
  • Neural hearing loss of left ear (1010229008)
  • Neural hearing loss of right ear (1010230003)
  • Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome (771308008)
  • Non-syndromic mitochondrial sensorineural deafness (1187512003)
  • Ocular albinism with late-onset sensorineural deafness (722054007)
  • Oculootodental syndrome (770944002)
  • Oculootoradial syndrome (722019000)
  • Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss (715483009)
  • Otodental syndrome (1237343009)
  • Ototoxicity - deafness (267677007)
  • Palmoplantar keratoderma with deafness syndrome (722203001)
  • Pendred's syndrome (70348004)
  • Perinatal sensorineural hearing loss (232331006)
  • Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (765325002)
  • Peripheral neuropathy with sensorineural hearing impairment syndrome (723497003)
  • Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (782752005)
  • Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (237612000)
  • Pili torti-deafness syndrome (67817003)
  • Postnatal acquired sensorineural hearing loss (232332004)
  • Postoperative profound sensorineural hearing loss (277424008)
  • Presbycusis (49526009)
  • Profound sensorineural hearing loss (700454004)
  • Profound sensorineural hearing loss (860841000000107)
  • Profound sensorineural hearing loss (890361000000100)
  • Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome (1237413006)
  • Progressive bulbar palsy with sensorineural deafness (699866005)
  • Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (719272007)
  • Proliferating cell nuclear antigen-related progressive neurodegenerative photosensitivity syndrome (1228871002)
  • Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness (236529001)
  • Recessive sensorineural hearing loss (232330007)
  • Renal caliceal diverticuli and deafness syndrome (782942003)
  • Renal tubular acidosis with progressive nerve deafness (236532003)
  • Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome (1172605003)
  • Retinitis pigmentosa-deafness syndrome (57838006)
  • Retinitis pigmentosa-deafness syndrome type 3 (1010610007)
  • Retinitis pigmentosa-deafness-ataxia syndrome (73119000)
  • Rubella deafness (186570004)
  • Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (721207002)
  • Sensorineural deafness and male infertility (700489002)
  • Sensorineural deafness due to late congenital syphilis (1142112002)
  • Sensorineural deafness with dilated cardiomyopathy syndrome (723993005)
  • Sensorineural hearing loss (60700002)
  • Sensorineural hearing loss (& [deafness: [high frequency] or [low frequency]) (194421002)
  • Sensorineural hearing loss of bilateral ears (194424005)
  • Sensorineural hearing loss of combined sites (65680009)
  • Sensorineural hearing loss of left ear (1119387004)
  • Sensorineural hearing loss of left ear with normal hearing on right side (1010442006)
  • Sensorineural hearing loss of right ear (1119386008)
  • Sensorineural hearing loss of right ear with normal hearing on left side (1010441004)
  • Sensorineural hearing loss, early graying, essential tremor syndrome (723721007)
  • Sensory hearing loss (85571008)
  • Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome (770751003)
  • Severe sensorineural hearing loss (860811000000106)
  • Severe sensorineural hearing loss (891401000000102)
  • Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome (716192009)
  • Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome (1284851009)
  • Spastic paraplegia, nephritis, deafness syndrome (733089005)
  • Split hand, split foot malformation with sensorineural hearing loss syndrome (723611008)
  • Split-foot malformation, mesoaxial polydactyly syndrome (1172635005)
  • Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome (718763005)
  • Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome (1356736002)
  • Stickler syndrome type 3 (783097004)
  • Sudden sensorineural hearing loss (715239002)
  • Syndromic sensorineural deafness due to combined oxidative phosphorylation defect (1260133007)
  • Temtamy preaxial brachydactyly syndrome (777998000)
  • Unilateral mixed conductive and sensorineural hearing loss with unrestricted hearing on the contralateral side (194428008)
  • Unilateral sensorineural hearing loss with unrestricted hearing on the contralateral side (194425006)
  • Usher syndrome type 1 (232057003)
  • Usher syndrome type 1F (514793471000119104)
  • Usher syndrome type 2 (232058008)
  • Waardenburg Shah syndrome (715952000)
  • Waardenburg syndrome type 3 (237918004)
  • Wildervanck syndrome (79665007)
  • Wolfram syndrome (70694009)
  • Wolfram syndrome type 1 (1285518004)
  • Wolfram syndrome type 2 (1285519007)
  • X-linked diffuse leiomyomatosis with Alport syndrome (726106004)
  • X-linked sensorineural hearing loss (232329002)
  • X-linked spinocerebellar ataxia type 3 (719817002)