Congenital myopathy 2c, severe infantile, autosomal dominant

Preferred Label : Congenital myopathy 2c, severe infantile, autosomal dominant;

Symbol : CMYO2C;

Type : Phenotype, molecular basis known;

Prefixed ID : #620278;

Details

Origin ID

620278;

UMLS CUI

C5830333;

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

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