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Summary Literature (0)
DOID:0060237 - Warburg micro syndrome

Disease Ontology Definition:An autosomal recessive disease characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism.

Synonyms: WARBM, Warburg-Sjo-Fledelius syndrome, micro syndrome,

Echinobase Genes : rab18, rab3gap1, tbc1d20

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

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