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


Disease Ontology Definition:n_a

Synonyms: HARD syndrome, cerebroocular dysplasia-muscular dystrophy syndrome

In OMIM:
OMIM:236670 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1
OMIM:253280 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3

In Mondo Disease Ontology:
MONDO:0019523 - Walker-Warburg syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : pomt1, pomgnt1, fkrp, fktn, pomgnt2, pomk, pomt2, b4gat1, rxylt1, b3galnt2, crppa, dag1, large1, col4a1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): congenital muscular dystrophy (is_a)