non-syndromic X-linked intellectual disability 72

Summary

DOID:0112059 - non-syndromic X-linked intellectual disability 72

Disease Ontology Definition:A non-syndromic X-linked intellectual disability that has_material_basis_in hemizygous mutation in the RAB39B gene on chromosome Xq28.

Synonyms: MRX72, X-linked mental retardation 72

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

: rab39b

MIM:

MIM:300271 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 72; XLID72

MIM:300271 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 72; XLID72

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

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

Parent(s): non-syndromic X-linked intellectual disability (is_a), X-linked recessive disease (is_a)