Disease #03599 (EDMD7 (dystrophy, muscular, Emery-Dreifuss, type 7, autosomal dominant (EDMD-7)), OMIM:614302)

Official abbreviation	EDMD7
Name	dystrophy, muscular, Emery-Dreifuss, type 7, autosomal dominant (EDMD-7)
OMIM ID	614302
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TMEM43
Associated tissues	-
Disease features	-
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