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

Official abbreviation EDMD-7
Name dystrophy, muscular, Emery-Dreifuss, type 7, autosomal dominant (EDMD-7)
OMIM ID 614302
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene TMEM43
Associated tissues -
Disease features -
Remarks -