Disease #05552 (CMH27 (cardiomyopathy, hypertrophic, familial, type 27 (CMH-27)), OMIM:618052)

Official abbreviation	CMH27
Name	cardiomyopathy, hypertrophic, familial, type 27 (CMH-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	autosomal recessive
Remarks	-
Date created	2019-01-22 14:56:50 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD