OMOP Concept 4172436
Hereditary motor neuron disease
StandardConditionSNOMED49793008Disorder
Maps from
3
Descendants
30
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Hereditary motor neuron disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138757 | Hereditary motor neuron disease | Non-standard |
| ICD10CM | G12.24 | Familial motor neuron disease | Non-standard |
| Nebraska Lexicon | 49793008 | Hereditary motor neuron disease | Non-standard |
Synonyms
Alternative names recorded for Hereditary motor neuron disease across source vocabularies.
- enfermedad familiar de la neurona motora
- enfermedad familiar de la neurona motora (trastorno)
- enfermedad hereditaria de la neurona motora
- Familial motor neuron disease
- Hereditary motor neuron disease (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(9)Roll up to these when you need a wider cohort.
Narrower concepts
(30)Included automatically when you query with descendants.
- 1Juvenile primary lateral sclerosis
- 1Neurogenic scapuloperoneal syndrome Kaeser type
- 1Spinal muscular atrophy
- 2Adult spinal muscular atrophy
- 2Autosomal dominant adult-onset proximal spinal muscular atrophy
- 2Bulbospinal neuronopathy
- 2Distal spinal muscular atrophy
- 2Facioscapulohumeral spinal muscular atrophy
- 2Hereditary canine spinal muscular atrophy
- 2Kugelberg-Welander disease
- 2Lower motor neuron syndrome with late-adult onset
- 2Oculopharyngeal spinal muscular atrophy
- 2Progressive bulbar palsy of childhood
- 2Scapulohumeral spinal muscular atrophy
- 2Scapuloperoneal spinal muscular atrophy
- 2Spinal atrophy, ophthalmoplegia, pyramidal syndrome
- 2Spinal muscular atrophy, type II
- 2Spinal muscular atrophy with lower extremity predominance
- 2Spinal muscular atrophy with progressive myoclonic epilepsy
- 2Werdnig-Hoffmann disease
- 2X-linked distal arthrogryposis multiplex congenita
- 3Autosomal dominant congenital benign spinal muscular atrophy
- 3Autosomal recessive lower motor neuron disease with childhood onset
- 3Distal hereditary motor neuropathy type 1
- 3Distal hereditary motor neuropathy type 7
- 3Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome
- 3Facioscapulohumeral spinal muscular atrophy with sensory loss
- 3Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome
- 3Spinal muscular atrophy with respiratory distress type 2
- 3X-linked distal spinal muscular atrophy type 3
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