OMOP Concept 36674792
Distal hereditary motor neuropathy type 1
StandardConditionSNOMED770630005Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2019
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Distal hereditary motor neuropathy type 1 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C566675 | Neuronopathy, Distal Hereditary Motor, Type I | Non-standard |
Synonyms
Alternative names recorded for Distal hereditary motor neuropathy type 1 across source vocabularies.
- Autosomal dominant distal juvenile spinal muscular atrophy type 1
- Distal hereditary motor neuropathy type 1 (disorder)
- neuropatía motora hereditaria distal tipo 1
- neuropatía motora hereditaria distal tipo 1 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Autosomal dominant distal hereditary motor neuropathy
- 1Distal spinal muscular atrophy
- 2Autosomal dominant hereditary disorder
- 2Hereditary disorder of nervous system
- 2Peripheral motor neuropathy
- 2Spinal muscular atrophy
- 3Autosomal hereditary disorder
- 3Chronic nervous system disorder
- 3Disorder of nervous system
- 3Disorder of the peripheral nervous system
- 3Hereditary disorder by system
- 3Hereditary motor neuron disease
- 3Lower motor neuron disease
- 3Neuropathy
- 4Chronic disease
- 4Disorder of body system
- 4Hereditary disease
- 4Motor neuron disease
- 5Disease
- 5Genetic disease
- 6Clinical finding
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