Disease #02366 (CMD1D;LVNC6 (cardiomyopathy, dilated, type 1D (CMD-1D); ventricular noncompaction, left, type 6 (LVNC-6)), OMIM:601494)

Official abbreviation	CMD1D;LVNC6
Name	cardiomyopathy, dilated, type 1D (CMD-1D); ventricular noncompaction, left, type 6 (LVNC-6)
OMIM ID	601494
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TNNT2
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)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.

Global Variome shared LOVD