Disease #05656 (LGMDD-4;LGMD-1I (dystrophy, muscular, limb-girdle, autosomal dominant, type 4 (LGMDD-4, LGMD-1I)), OMIM:618129)

Official abbreviation LGMDD-4;LGMD-1I
Name dystrophy, muscular, limb-girdle, autosomal dominant, type 4 (LGMDD-4, LGMD-1I)
OMIM ID 618129
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CAPN3
Associated tissues -
Disease features -
Remarks autosomal dominant