Disease #07225 (CSMH (hamartoma, smooth muscle, congenital, with/without hemihypertrophy), OMIM:620470)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CSMH
Name	hamartoma, smooth muscle, congenital, with/without hemihypertrophy
OMIM ID	620470
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ACTB
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-12-28 16:54:53 +01:00 (CET)
Date last edited	N/A

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