Disease #05852 (MDDGB15 (dystrophy, muscular, dystroglycanopathy (congenital with impaired intellectual development), type B15 (MDDGB15)), OMIM:618992)

Official abbreviation MDDGB15
Name dystrophy, muscular, dystroglycanopathy (congenital with impaired intellectual development), type B15 (MDDGB15)
OMIM ID 618992
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene DPM3
Associated tissues -
Disease features -
Remarks -