Disease #01088

Official abbreviation LGMD-2O;MDDGC-3
Name dystrophy, muscular, limb-girdle, type 2O (LGMD-2O, dystroglycanopathy C3 (MDDGC-3))
OMIM ID 613157
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 -