Disease #01097 (MDDGA-4;MEB;WWS (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A4 (MDDGA-4, Walker-Warburg syndrome (WWS), muscle-eye-brain disease (MEB))), OMIM:253800)

Official abbreviation MDDGA-4;MEB;WWS
Name dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A4 (MDDGA-4, Walker-Warburg syndrome (WWS), muscle-eye-brain disease (MEB))
OMIM ID 253800
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 -