Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:253280 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3

Xenbase Genes: pomgnt1, fkrp

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000171 - muscular dystrophy-dystroglycanopathy, type A
MONDO:0009667 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3
MONDO:0018939 - muscle-eye-brain disease

Disease Ontology (DO):
DOID:0050560 - Walker-Warburg syndrome