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Echinobase
Summary Literature (0)
DOID:0050560 - Walker-Warburg syndrome

Disease Ontology Definition:n_a

Synonyms: HARD syndrome, cerebroocular dysplasia-muscular dystrophy syndrome,

Echinobase Genes : pomgnt1, pomt1, pomt2


OMIM:
MIM:236670 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1; mddga1
MIM:253280 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3; mddga3

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): congenital muscular dystrophy (is_a)