Congenital myopathy 22b, severe fetal

Preferred Label : Congenital myopathy 22b, severe fetal;

Symbol : CMYO22B;

Type : Phenotype, molecular basis known;

Prefixed ID : #620369;

Détails

Origin ID

620369;

UMLS CUI

C5830501;

Genes related to phenotype
- Sodium voltage-gated channel, alpha subunit 4 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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