Neuronopathy, distal hereditary motor, autosomal dominant 10

Preferred Label : Neuronopathy, distal hereditary motor, autosomal dominant 10;

Symbol : HMND10;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Neuropathy, distal hereditary motor, type X; DHMN10; HMN10; Neuronopathy, distal hereditary motor, type X;

Prefixed ID : #620080;

Details

Origin ID

620080;

UMLS CUI

C5774234;

Genes related to phenotype
- Elastin microfibril interfacer 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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