neuronopathy, distal hereditary motor, type viib

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

MeSH synonym : HMN VIIB; neuropathy, distal hereditary motor, type VIIB; HMN7B; lower motor neuron disease, dynactin type; neuropathy, distal hereditary motor, with vocal cord paralysis, type VIIB;

Details

Origin ID

C564362;

UMLS CUI

C1843315;

Automatic exact mappings (from CISMeF team)
- distal hereditary motor neuronopathy type 7B [DO Concept]
Currated CISMeF NLP mapping
- Neuronopathy, distal hereditary motor, autosomal dominant 14 [OMIM Phenotype]
MeSH term(s) associated for indexing
- muscular atrophy, spinal [MeSH Descriptor]
Record concept(s)
- neuronopathy, distal hereditary motor, type viib [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Neuronopathy, distal hereditary motor, autosomal dominant 14 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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