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Summary Literature (3)
DOID:0080694 - Galloway-Mowat syndrome

Disease Ontology Definition:A syndrome that is characterized by developmental delay, progressive microcephaly, cerebral and cerebellar atrophy with extrapyramidal involvement, and optic atrophy.

Synonyms:

Xenbase Genes : tp53rk, osgep, znf592, nup133, nup107, tprkb, wdr73, lage3, wdr4



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

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