Neuronopathy, distal hereditary motor, autosomal recessive 10

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

Symbol : HMNR10;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Vrk1-related motor neuron disease; Neuropathy, distal hereditary motor, autosomal recessive 10;

Prefixed ID : #620542;

Détails

Origin ID

620542;

UMLS CUI

C5882703;

Genes related to phenotype
- Vrk serine/threonine kinase 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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