Disease #01087

Official abbreviation MDDGB-3
Name dystrophy, muscular, dystroglycanopathy (congenital with mental retardation), type B3 (MDDGB-3)
OMIM ID 613151
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene POMGNT1
Associated tissues -
Disease features -
Remarks -