Congenital smooth muscle hamartoma, with or without hemihypertrophy

Preferred Label : Congenital smooth muscle hamartoma, with or without hemihypertrophy;

Symbol : CSMH;

Type : Phenotype, molecular basis known;

Prefixed ID : #620470;

Details

Origin ID

620470;

UMLS CUI

C5882676;

Genes related to phenotype
- Actin, beta [OMIM gene]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]

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