Disease #05551 (CMH26;RCM5 (cardiomyopathy, hypertrophic, type 26 (CMD-26); cardiomyopathy, restrictive, type 5 (RCM-5)), OMIM:617047)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CMH26;RCM5
Name	cardiomyopathy, hypertrophic, type 26 (CMD-26); cardiomyopathy, restrictive, type 5 (RCM-5)
OMIM ID	617047
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FLNC
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2019-01-22 14:54:52 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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