Disease #03292 (CMH14 (cardiomyopathy, hypertrophic, familial, type 14), OMIM:613251)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CMH14
Name	cardiomyopathy, hypertrophic, familial, type 14
OMIM ID	613251
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MYH6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2023-10-01 20:53:44 +02:00 (CEST)

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