Disease #00218 (CMH27 (CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 27), OMIM:618052)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
Log in

Official abbreviation	CMH27
Name	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 27
OMIM ID	618052
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ALPK3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-09-09 10:12:10 +00:00 (UTC)
Date last edited	N/A