Disease #00073

Official abbreviation MDDGA-3;MEB;WWS
Name dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A3 (MDDGA-3, Walker-Warburg syndrome (WWS), muscle-eye-brain disease (MEB))
OMIM ID 253280
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 -