Warburg micro syndrome 3

Summary

DOID:0110718 - Warburg micro syndrome 3

Disease Ontology Definition:A Warburg micro syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB18 gene on chromosome 10p12.

Synonyms: Micro Syndrome 3, WARBM3

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

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013638 - Warburg micro syndrome 3

MONDO:0013638 - Warburg micro syndrome 3

MIM:

MIM:614222 - WARBURG MICRO SYNDROME 3; WARBM3

MIM:614222 - WARBURG MICRO SYNDROME 3; WARBM3

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)