Congenital myopathy 2b, severe infantile, autosomal recessive

Preferred Label : Congenital myopathy 2b, severe infantile, autosomal recessive;

Symbol : CMYP2B;

Type : Phenotype, molecular basis known;

Prefixed ID : #620265;

Details

Origin ID

620265;

UMLS CUI

C5830300;

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

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