neuronopathy, distal hereditary motor, type I

Preferred Label : neuronopathy, distal hereditary motor, type I;

MeSH synonym : spinal muscular atrophy, distal, juvenile, autosomal dominant, I; Charcot-Marie-Tooth disease, spinal, I; neuropathy, distal hereditary motor, type I;

Details

Origin ID

C566675;

UMLS CUI

C1866784;

Currated CISMeF NLP mapping
- Distal Hereditary Motor Neuronopathy Type I [NCIt concept]
- Distal hereditary motor neuropathy type 1 [ORDO Disease]
- Distal hereditary motor neuropathy type 1 [ICD-11 More detail]
- Distal hereditary motor neuropathy type 1 (disorder) [SNOMED CT concept]
- Neuronopathy, distal hereditary motor, autosomal dominant 1 [OMIM Phenotype]
- distal hereditary motor neuronopathy type 1 [DO Concept]
DO Cross reference
- distal hereditary motor neuronopathy type 1 [DO Concept]
MeSH term(s) associated for indexing
- muscular atrophy, spinal [MeSH Descriptor]
Record concept(s)
- neuronopathy, distal hereditary motor, type I [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Distal Hereditary Motor Neuronopathy Type I [NCIt concept]
- Distal hereditary motor neuropathy type 1 [ORDO Disease]
- Distal hereditary motor neuropathy type 1 (disorder) [SNOMED CT concept]
- Neuronopathy, distal hereditary motor, autosomal dominant 1 [OMIM Phenotype]
- distal hereditary motor neuronopathy type 1 [DO Concept]

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