Motor Neurone Disease (SNOMED CT)

Coding system: SNOMED CT (UK Clinical Edition)
Coding system release: unknown
Organisation: NHS Digital
Codelist ID: nhsd/motor-neurone-disease-snomed-ct
Version ID: 5a2739f8
Number of codes included: 32

Versions

Description

Taken from the Motor Neurone Disease tab of the Population Risk COVID-19 Treatments code list v1.3, published by NHS Digital, 2021-12-13.

References

NHSD Population Risk COVID-19 Treatments

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.

Search:

code	term
7379000	Pseudobulbar palsy
37340000	Motor neuron disease
46251005	Corticospinal motor disease
49793008	Hereditary motor neuron disease
54304004	Progressive bulbar palsy
81211007	Primary lateral sclerosis
84590007	Lower motor neuron disease
85672005	Anterior horn cell disease
86044005	Amyotrophic lateral sclerosis
88923002	Progressive muscular atrophy
230246005	Progressive bulbar palsy of childhood
230253001	Bulbospinal neuronopathy
230254007	Western Pacific motor neurone disease
230255008	Madras-type motor neurone disease
230257000	Paraneoplastic motor neurone disease
230258005	Amyotrophic lateral sclerosis with dementia
230274000	Frontal lobe degeneration with motor neurone disease
230784003	Congenital pseudobulbar palsy
249892007	Progressive pseudobulbar palsy
398432008	Bulbar weakness
699866005	Progressive bulbar palsy with sensorineural deafness
715565004	Lethal arthrogryposis co-occurrent with anterior horn cell disease
717964007	Juvenile primary lateral sclerosis
718555006	Juvenile amyotrophic lateral sclerosis
722987009	Amyotrophic lateral sclerosis plus syndrome
771302009	Autosomal recessive lower motor neuron disease with childhood onset
783618006	Lower motor neuron syndrome with late-adult onset
784341001	Amyotrophic lateral sclerosis type 4
838276009	Amyotrophic lateral sclerosis, parkinsonism, dementia complex
583151000000109	Other anterior horn cell disease
630471000000103	Anterior horn cell disease NOS
646201000000105	Motor neurone disease NOS

Showing 1 to 32 of 32 entries

Disorder

Status:
Included
Name:
Motor neuron disease
Code:
(37340000)
- Status:
  Included
  Name:
  Amyotrophic lateral sclerosis
  Code:
  (86044005)
  - Status:
    Included
    Name:
    Amyotrophic lateral sclerosis plus syndrome
    Code:
    (722987009)
  - Status:
    Included
    Name:
    Amyotrophic lateral sclerosis type 4
    Code:
    (784341001)
  - Status:
    Included
    Name:
    Amyotrophic lateral sclerosis with dementia
    Code:
    (230258005)
  - Status:
    Included
    Name:
    Amyotrophic lateral sclerosis, parkinsonism, dementia complex
    Code:
    (838276009)
  - Status:
    Included
    Name:
    Juvenile amyotrophic lateral sclerosis
    Code:
    (718555006)
- Status:
  Included
  Name:
  Frontal lobe degeneration with motor neurone disease
  Code:
  (230274000)
- Status:
  Included
  Name:
  Hereditary motor neuron disease
  Code:
  (49793008)
  - Status:
    Included
    Name:
    Juvenile primary lateral sclerosis
    Code:
    (717964007)
  - Status:
    Excluded
    Name:
    Spinal muscular atrophy
    Code:
    (5262007)
    Status:
    Excluded
    Name:
    Adult spinal muscular atrophy
    Code:
    (85505000)
    Status:
    Excluded
    Name:
    Autosomal dominant adult-onset proximal spinal muscular atrophy
    Code:
    (784391002)
    Status:
    Excluded
    Name:
    Autosomal dominant childhood-onset proximal spinal muscular atrophy
    Code:
    (772129007)
    Status:
    Included
    Name:
    Bulbospinal neuronopathy
    Code:
    (230253001)
    Status:
    Excluded
    Name:
    Distal spinal muscular atrophy
    Code:
    (230247001)
    Status:
    Excluded
    Name:
    Autosomal dominant congenital benign spinal muscular atrophy
    Code:
    (763067000)
    Status:
    Excluded
    Name:
    Autosomal recessive distal spinal muscular atrophy type 3
    Code:
    (770430000)
    Status:
    Included
    Name:
    Autosomal recessive lower motor neuron disease with childhood onset
    Code:
    (771302009)
    Status:
    Excluded
    Name:
    Distal hereditary motor neuropathy Jerash type
    Code:
    (763533003)
    Status:
    Excluded
    Name:
    Distal hereditary motor neuropathy type 1
    Code:
    (770630005)
    Status:
    Excluded
    Name:
    Distal hereditary motor neuropathy type 7
    Code:
    (771081007)
    Status:
    Excluded
    Name:
    Spinal muscular atrophy with respiratory distress type 1
    Code:
    (711483003)
    Status:
    Excluded
    Name:
    Spinal muscular atrophy with respiratory distress type 2
    Code:
    (770727008)
    Status:
    Excluded
    Name:
    Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome
    Code:
    (723612001)
    Status:
    Excluded
    Name:
    X-linked distal spinal muscular atrophy type 3
    Code:
    (766764008)
    Status:
    Excluded
    Name:
    Young adult-onset distal hereditary motor neuropathy
    Code:
    (771475006)
    Status:
    Excluded
    Name:
    Facioscapulohumeral spinal muscular atrophy
    Code:
    (230249003)
    Status:
    Excluded
    Name:
    Facioscapulohumeral spinal muscular atrophy with sensory loss
    Code:
    (230250003)
    Status:
    Excluded
    Name:
    Kugelberg-Welander disease
    Code:
    (54280009)
    Status:
    Included
    Name:
    Lower motor neuron syndrome with late-adult onset
    Code:
    (783618006)
    Status:
    Excluded
    Name:
    Oculopharyngeal spinal muscular atrophy
    Code:
    (230252006)
    Status:
    Included
    Name:
    Progressive bulbar palsy of childhood
    Code:
    (230246005)
    Status:
    Excluded
    Name:
    Scapulohumeral spinal muscular atrophy
    Code:
    (230251004)
    Status:
    Excluded
    Name:
    Scapuloperoneal spinal muscular atrophy
    Code:
    (230248006)
    Status:
    Excluded
    Name:
    Spinal atrophy, ophthalmoplegia, pyramidal syndrome
    Code:
    (771238004)
    Status:
    Excluded
    Name:
    Spinal muscular atrophy with progressive myoclonic epilepsy
    Code:
    (703524005)
    Status:
    Excluded
    Name:
    Spinal muscular atrophy, type II
    Code:
    (128212001)
    Status:
    Excluded
    Name:
    Werdnig-Hoffmann disease
    Code:
    (64383006)
    Status:
    Excluded
    Name:
    X-linked distal arthrogryposis multiplex congenita
    Code:
    (719836007)
- Status:
  Included
  Name:
  Lower motor neuron disease
  Code:
  (84590007)
  - Status:
    Included
    Name:
    Anterior horn cell disease
    Code:
    (85672005)
    Status:
    Included
    Name:
    Lethal arthrogryposis co-occurrent with anterior horn cell disease
    Code:
    (715565004)
    Status:
    Excluded
    Name:
    Werdnig-Hoffmann disease
    Code:
    (64383006)
  - Status:
    Excluded
    Name:
    Spinal muscular atrophy
    Code:
    (5262007)
    Status:
    Excluded
    Name:
    Adult spinal muscular atrophy
    Code:
    (85505000)
    Status:
    Excluded
    Name:
    Autosomal dominant adult-onset proximal spinal muscular atrophy
    Code:
    (784391002)
    Status:
    Excluded
    Name:
    Autosomal dominant childhood-onset proximal spinal muscular atrophy
    Code:
    (772129007)
    Status:
    Included
    Name:
    Bulbospinal neuronopathy
    Code:
    (230253001)
    Status:
    Excluded
    Name:
    Distal spinal muscular atrophy
    Code:
    (230247001)
    Status:
    Excluded
    Name:
    Autosomal dominant congenital benign spinal muscular atrophy
    Code:
    (763067000)
    Status:
    Excluded
    Name:
    Autosomal recessive distal spinal muscular atrophy type 3
    Code:
    (770430000)
    Status:
    Included
    Name:
    Autosomal recessive lower motor neuron disease with childhood onset
    Code:
    (771302009)
    Status:
    Excluded
    Name:
    Distal hereditary motor neuropathy Jerash type
    Code:
    (763533003)
    Status:
    Excluded
    Name:
    Distal hereditary motor neuropathy type 1
    Code:
    (770630005)
    Status:
    Excluded
    Name:
    Distal hereditary motor neuropathy type 7
    Code:
    (771081007)
    Status:
    Excluded
    Name:
    Spinal muscular atrophy with respiratory distress type 1
    Code:
    (711483003)
    Status:
    Excluded
    Name:
    Spinal muscular atrophy with respiratory distress type 2
    Code:
    (770727008)
    Status:
    Excluded
    Name:
    Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome
    Code:
    (723612001)
    Status:
    Excluded
    Name:
    X-linked distal spinal muscular atrophy type 3
    Code:
    (766764008)
    Status:
    Excluded
    Name:
    Young adult-onset distal hereditary motor neuropathy
    Code:
    (771475006)
    Status:
    Excluded
    Name:
    Facioscapulohumeral spinal muscular atrophy
    Code:
    (230249003)
    Status:
    Excluded
    Name:
    Facioscapulohumeral spinal muscular atrophy with sensory loss
    Code:
    (230250003)
    Status:
    Excluded
    Name:
    Kugelberg-Welander disease
    Code:
    (54280009)
    Status:
    Included
    Name:
    Lower motor neuron syndrome with late-adult onset
    Code:
    (783618006)
    Status:
    Excluded
    Name:
    Oculopharyngeal spinal muscular atrophy
    Code:
    (230252006)
    Status:
    Included
    Name:
    Progressive bulbar palsy of childhood
    Code:
    (230246005)
    Status:
    Excluded
    Name:
    Scapulohumeral spinal muscular atrophy
    Code:
    (230251004)
    Status:
    Excluded
    Name:
    Scapuloperoneal spinal muscular atrophy
    Code:
    (230248006)
    Status:
    Excluded
    Name:
    Spinal atrophy, ophthalmoplegia, pyramidal syndrome
    Code:
    (771238004)
    Status:
    Excluded
    Name:
    Spinal muscular atrophy with progressive myoclonic epilepsy
    Code:
    (703524005)
    Status:
    Excluded
    Name:
    Spinal muscular atrophy, type II
    Code:
    (128212001)
    Status:
    Excluded
    Name:
    Werdnig-Hoffmann disease
    Code:
    (64383006)
    Status:
    Excluded
    Name:
    X-linked distal arthrogryposis multiplex congenita
    Code:
    (719836007)
- Status:
  Included
  Name:
  Madras-type motor neurone disease
  Code:
  (230255008)
- Status:
  Excluded
  Name:
  Mills syndrome
  Code:
  (785809005)
- Status:
  Excluded
  Name:
  Motor neuron disease due to lead intoxication
  Code:
  (866051002)
- Status:
  Excluded
  Name:
  Neuromyotonia
  Code:
  (305719002)
  - Status:
    Excluded
    Name:
    Autosomal recessive axonal neuropathy with neuromyotonia
    Code:
    (711406009)
- Status:
  Included
  Name:
  Paraneoplastic motor neurone disease
  Code:
  (230257000)
- Status:
  Included
  Name:
  Progressive muscular atrophy
  Code:
  (88923002)
  - Status:
    Excluded
    Name:
    Post poliomyelitis syndrome
    Code:
    (31097004)
- Status:
  Excluded
  Name:
  Spastic tetraplegia with rigidity syndrome
  Code:
  (44395000)
- Status:
  Excluded
  Name:
  Troyer syndrome
  Code:
  (230264003)
- Status:
  Excluded
  Name:
  Upper motor neuron disease
  Code:
  (95647008)
  - Status:
    Included
    Name:
    Bulbar weakness
    Code:
    (398432008)
  - Status:
    Included
    Name:
    Corticospinal motor disease
    Code:
    (46251005)
  - Status:
    Included
    Name:
    Primary lateral sclerosis
    Code:
    (81211007)
    Status:
    Included
    Name:
    Juvenile primary lateral sclerosis
    Code:
    (717964007)
  - Status:
    Included
    Name:
    Progressive bulbar palsy
    Code:
    (54304004)
    Status:
    Included
    Name:
    Progressive bulbar palsy of childhood
    Code:
    (230246005)
    Status:
    Included
    Name:
    Progressive bulbar palsy with sensorineural deafness
    Code:
    (699866005)
  - Status:
    Included
    Name:
    Pseudobulbar palsy
    Code:
    (7379000)
    Status:
    Excluded
    Name:
    Anterior opercular syndrome
    Code:
    (864471000000106)
    Status:
    Included
    Name:
    Congenital pseudobulbar palsy
    Code:
    (230784003)
    Status:
    Included
    Name:
    Progressive pseudobulbar palsy
    Code:
    (249892007)
- Status:
  Included
  Name:
  Western Pacific motor neurone disease
  Code:
  (230254007)

[Inactive] Disorder

Status:
Included
Name:
Anterior horn cell disease NOS
Code:
(630471000000103)
Status:
Included
Name:
Motor neurone disease NOS
Code:
(646201000000105)
Status:
Included
Name:
Other anterior horn cell disease
Code:
(583151000000109)