Warburg micro syndrome

Summary

DOID:0060237 - Warburg micro syndrome

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

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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: rab18, tbc1d20, rab3gap2, rab3gap1, tbc1d20.2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0016649 - Warburg micro syndrome

MONDO:0016649 - Warburg micro syndrome

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), syndrome (is_a)