Disease #01098 (MDDGB-4 (dystrophy, muscular, dystroglycanopathy (congenital without mental retardation), type B4 (MDDGB-4)), OMIM:613152)

Official abbreviation MDDGB-4
Name dystrophy, muscular, dystroglycanopathy (congenital without mental retardation), type B4 (MDDGB-4)
OMIM ID 613152
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FKTN
Associated tissues -
Disease features -
Remarks -