Warburg micro syndrome 1

Summary

DOID:0110716 - Warburg micro syndrome 1

Disease Ontology Definition:A Warburg micro syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP1 gene on chromosome 2q21.

Synonyms: Micro Syndrome 1, WARBM1

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

: rab3gap1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010822 - Warburg micro syndrome 1

MONDO:0010822 - Warburg micro syndrome 1

MIM:

MIM:600118 - WARBURG MICRO SYNDROME 1; WARBM1

MIM:600118 - WARBURG MICRO SYNDROME 1; WARBM1

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

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

Parent(s): Warburg micro syndrome (is_a)