Neuronopathy, distal hereditary motor, autosomal dominant 11

Preferred Label : Neuronopathy, distal hereditary motor, autosomal dominant 11;

Symbol : HMND11;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Neuropathy, distal hereditary motor, 11; DHMN11;

Prefixed ID : #620528;

Details

Origin ID

620528;

UMLS CUI

C5882697;

Genes related to phenotype
- Spectrin, alpha, nonerythrocytic 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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