Disease #03914 (CMD1LL;LVNC8 (cardiomyopathy, dilated, type 1LL (CMD-1LL); ventricular noncompaction, left, type 8 (LVNC-8)), OMIM:615373)

Official abbreviation	CMD1LL;LVNC8
Name	cardiomyopathy, dilated, type 1LL (CMD-1LL); ventricular noncompaction, left, type 8 (LVNC-8)
OMIM ID	615373
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PRDM16
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD