Congenital myopathy 21 with early respiratory failure

Preferred Label : Congenital myopathy 21 with early respiratory failure;

Symbol : CMYO21;

Type : Phenotype, molecular basis known;

Prefixed ID : #620326;

Details

Origin ID

620326;

UMLS CUI

C5830424;

Genes related to phenotype
- Dnaj/hsp40 homolog, subfamily b, member 4 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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