has_mnd_ms_myas_or_huntingtons

Codelist metadata

Coding system
SNOMED CT (UK Clinical Edition)
Coding system release
unknown
Organisation
QCovid
Codelist ID
qcovid/has_mnd_ms_myas_or_huntingtons
Version ID
4b70c3f1
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Versions

  1. 4b70c3f1 Published
    Created: 18 Mar 2021 at 09:27

About

Description

SNOMED codelist for the has_mnd_ms_myas_or_huntingtons group in the QCovid® to develop the COVID-19 Population Risk Assessment.

References

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.

Disorder

  • Status:
    Included
    Name:
    Huntington's chorea
    Code:
    (58756001)
    • Status:
      Excluded
      Name:
      Akinetic-rigid form of Huntington's disease
      Code:
      (230301006)
    • Status:
      Excluded
      Name:
      Juvenile onset Huntington's disease
      Code:
      (230299004)
    • Status:
      Excluded
      Name:
      Late onset Huntington's disease
      Code:
      (230300007)
  • Status:
    Included
    Name:
    Motor neuron disease
    Code:
    (37340000)
    • Status:
      Included
      Name:
      Amyotrophic lateral sclerosis
      Code:
      (86044005)
      • Status:
        Excluded
        Name:
        Amyotrophic lateral sclerosis plus syndrome
        Code:
        (722987009)
      • Status:
        Excluded
        Name:
        Amyotrophic lateral sclerosis type 4
        Code:
        (784341001)
      • Status:
        Included
        Name:
        Amyotrophic lateral sclerosis with dementia
        Code:
        (230258005)
      • Status:
        Excluded
        Name:
        Amyotrophic lateral sclerosis, parkinsonism, dementia complex
        Code:
        (838276009)
      • Status:
        Excluded
        Name:
        Juvenile amyotrophic lateral sclerosis
        Code:
        (718555006)
    • Status:
      Excluded
      Name:
      Frontal lobe degeneration with motor neurone disease
      Code:
      (230274000)
    • Status:
      Excluded
      Name:
      Hereditary motor neuron disease
      Code:
      (49793008)
      • Status:
        Excluded
        Name:
        Juvenile primary lateral sclerosis
        Code:
        (717964007)
      • Status:
        Included
        Name:
        Spinal muscular atrophy
        Code:
        (5262007)
        • Status:
          Included
          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:
          Included
          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:
            Excluded
            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:
          Included
          Name:
          Facioscapulohumeral spinal muscular atrophy
          Code:
          (230249003)
          • Status:
            Included
            Name:
            Facioscapulohumeral spinal muscular atrophy with sensory loss
            Code:
            (230250003)
        • Status:
          Included
          Name:
          Kugelberg-Welander disease
          Code:
          (54280009)
        • Status:
          Excluded
          Name:
          Lower motor neuron syndrome with late-adult onset
          Code:
          (783618006)
        • Status:
          Included
          Name:
          Oculopharyngeal spinal muscular atrophy
          Code:
          (230252006)
        • Status:
          Included
          Name:
          Progressive bulbar palsy of childhood
          Code:
          (230246005)
        • Status:
          Included
          Name:
          Scapulohumeral spinal muscular atrophy
          Code:
          (230251004)
        • Status:
          Included
          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:
          Included
          Name:
          Spinal muscular atrophy, type II
          Code:
          (128212001)
        • Status:
          Included
          Name:
          Werdnig-Hoffmann disease
          Code:
          (64383006)
        • Status:
          Excluded
          Name:
          X-linked distal arthrogryposis multiplex congenita
          Code:
          (719836007)
    • Status:
      Excluded
      Name:
      Lower motor neuron disease
      Code:
      (84590007)
      • Status:
        Included
        Name:
        Anterior horn cell disease
        Code:
        (85672005)
        • Status:
          Excluded
          Name:
          Lethal arthrogryposis co-occurrent with anterior horn cell disease
          Code:
          (715565004)
        • Status:
          Included
          Name:
          Werdnig-Hoffmann disease
          Code:
          (64383006)
      • Status:
        Included
        Name:
        Spinal muscular atrophy
        Code:
        (5262007)
        • Status:
          Included
          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:
          Included
          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:
            Excluded
            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:
          Included
          Name:
          Facioscapulohumeral spinal muscular atrophy
          Code:
          (230249003)
          • Status:
            Included
            Name:
            Facioscapulohumeral spinal muscular atrophy with sensory loss
            Code:
            (230250003)
        • Status:
          Included
          Name:
          Kugelberg-Welander disease
          Code:
          (54280009)
        • Status:
          Excluded
          Name:
          Lower motor neuron syndrome with late-adult onset
          Code:
          (783618006)
        • Status:
          Included
          Name:
          Oculopharyngeal spinal muscular atrophy
          Code:
          (230252006)
        • Status:
          Included
          Name:
          Progressive bulbar palsy of childhood
          Code:
          (230246005)
        • Status:
          Included
          Name:
          Scapulohumeral spinal muscular atrophy
          Code:
          (230251004)
        • Status:
          Included
          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:
          Included
          Name:
          Spinal muscular atrophy, type II
          Code:
          (128212001)
        • Status:
          Included
          Name:
          Werdnig-Hoffmann disease
          Code:
          (64383006)
        • Status:
          Excluded
          Name:
          X-linked distal arthrogryposis multiplex congenita
          Code:
          (719836007)
    • Status:
      Excluded
      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:
      Included
      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:
        Included
        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:
        Excluded
        Name:
        Bulbar weakness
        Code:
        (398432008)
      • Status:
        Excluded
        Name:
        Corticospinal motor disease
        Code:
        (46251005)
      • Status:
        Included
        Name:
        Primary lateral sclerosis
        Code:
        (81211007)
        • Status:
          Excluded
          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:
          Excluded
          Name:
          Progressive bulbar palsy with sensorineural deafness
          Code:
          (699866005)
      • Status:
        Included
        Name:
        Pseudobulbar palsy
        Code:
        (7379000)
        • Status:
          Included
          Name:
          Anterior opercular syndrome
          Code:
          (864471000000106)
        • Status:
          Included
          Name:
          Congenital pseudobulbar palsy
          Code:
          (230784003)
        • Status:
          Included
          Name:
          Progressive pseudobulbar palsy
          Code:
          (249892007)
    • Status:
      Excluded
      Name:
      Western Pacific motor neurone disease
      Code:
      (230254007)
  • Status:
    Included
    Name:
    Myasthenia gravis
    Code:
    (91637004)
    • Status:
      Included
      Name:
      Generalized myasthenia
      Code:
      (230686005)
    • Status:
      Included
      Name:
      Genetically determined myasthenia
      Code:
      (230669004)
      • Status:
        Included
        Name:
        Abnormality of synaptic vesicles
        Code:
        (230679002)
      • Status:
        Included
        Name:
        Congenital myasthenic syndrome
        Code:
        (230672006)
        • Status:
          Included
          Name:
          Acetylcholine resynthesis deficiency
          Code:
          (230671004)
        • Status:
          Included
          Name:
          Congenital end-plate acetylcholine receptor deficiency
          Code:
          (230673001)
        • Status:
          Included
          Name:
          Congenital end-plate acetylcholinesterase deficiency
          Code:
          (230677000)
        • Status:
          Excluded
          Name:
          Familial infantile myasthenia
          Code:
          (230670003)
      • Status:
        Included
        Name:
        Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency
        Code:
        (230678005)
      • Status:
        Included
        Name:
        Pseudomyopathic myasthenia
        Code:
        (230674007)
      • Status:
        Included
        Name:
        Putative defect in acetylcholine synthesis or packaging
        Code:
        (230676009)
    • Status:
      Included
      Name:
      Juvenile or adult myasthenia gravis
      Code:
      (193207007)
    • Status:
      Included
      Name:
      Myasthenia gravis associated with thymoma
      Code:
      (230685009)
    • Status:
      Excluded
      Name:
      Myasthenia gravis with exacerbation
      Code:
      (77461000119109)
    • Status:
      Excluded
      Name:
      Myasthenia gravis without exacerbation
      Code:
      (77471000119103)
    • Status:
      Excluded
      Name:
      Myasthenia gravis, adult form
      Code:
      (31839002)
    • Status:
      Excluded
      Name:
      Myasthenia gravis, juvenile form
      Code:
      (55051001)
      • Status:
        Included
        Name:
        Acetylcholine resynthesis deficiency
        Code:
        (230671004)
      • Status:
        Excluded
        Name:
        Familial infantile myasthenia
        Code:
        (230670003)
    • Status:
      Excluded
      Name:
      Myasthenic crisis
      Code:
      (80976008)
    • Status:
      Excluded
      Name:
      Neonatal myasthenia gravis
      Code:
      (82178003)
      • Status:
        Included
        Name:
        Persistent neonatal myasthenia gravis
        Code:
        (193206003)
      • Status:
        Excluded
        Name:
        Transient neonatal myasthenia
        Code:
        (230683002)
    • Status:
      Excluded
      Name:
      Ocular myasthenia
      Code:
      (230684008)
      • Status:
        Excluded
        Name:
        Ocular myasthenia with strabismus
        Code:
        (414927004)
    • Status:
      Excluded
      Name:
      Rippling muscle disease with myasthenia gravis
      Code:
      (770596007)

[Inactive] Disorder

  • Status:
    Included
    Name:
    Congenital and developmental myasthenia
    Code:
    (193216006)