Disease #05553 (CMD2C (cardiomyopathy, dialted, type 2C (CMD-2C)), OMIM:618189)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CMD2C
Name	cardiomyopathy, dialted, type 2C (CMD-2C)
OMIM ID	618189
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PPCS
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2019-01-22 15:09:08 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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