Disease #00198 (CMD1O (CARDIOMYOPATHY, DILATED, 1O), OMIM:608569)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	CMD1O
Name	CARDIOMYOPATHY, DILATED, 1O
OMIM ID	608569
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ABCC9
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-10-02 09:12:16 +00:00 (UTC)
Date last edited	2023-10-02 09:12:37 +00:00 (UTC)