Disease #00154 (CMH4 (CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4), OMIM:115197)

Official abbreviation	CMH4
Name	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4
OMIM ID	115197
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MYBPC3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-27 09:22:12 +00:00 (UTC)
Date last edited	N/A

MVZ für Humangenetik Regensburg