neuronopathy, distal hereditary motor, type V

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

MeSH note : PROM;

CISMeF acronym : DHMN V; DHMN5;

MeSH synonym : DHMN5; DSMAV; spinal muscular atrophy, distal, with upper limb predominance; HMN5; neuropathy, distal hereditary motor, type V; spinal muscular atrophy, distal, type V; DHMN V; HMN V; Dhmn-V; distal hereditary motor neuronopathy, type V; distal hereditary motor neuropathy, type V; spinal muscular atrophy, distal type V; distal spinal muscular atrophy, type V;

Details

Origin ID

C563443;

UMLS CUI

C1833308;

Currated CISMeF NLP mapping
- Distal hereditary motor neuropathy type 5 [ORDO Disease]
- Distal hereditary motor neuropathy type 5 (disorder) [SNOMED CT concept]
- Neuronopathy, distal hereditary motor, autosomal dominant 5 [OMIM Phenotype]
DO Cross reference
- distal hereditary motor neuronopathy type 5A [DO Concept]
MeSH term(s) associated for indexing
- muscular atrophy, spinal [MeSH Descriptor]
Record concept(s)
- neuronopathy, distal hereditary motor, type V [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Distal hereditary motor neuropathy type 5 [ORDO Disease]
- Distal hereditary motor neuropathy type 5 (disorder) [SNOMED CT concept]
- Neuronopathy, distal hereditary motor, autosomal dominant 5 [OMIM Phenotype]
- distal hereditary motor neuronopathy type 5A [DO Concept]

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