non-syndromic X-linked intellectual disability 101

Summary

DOID:0112048 - non-syndromic X-linked intellectual disability 101

Disease Ontology Definition:A non-syndromic X-linked intellectual disability characterized by global developmental delay that has_material_basis_in hemizygous mutation in the MID2 gene on chromosome Xq22.3.

Synonyms: MRX101, X-linked mental retardation 101

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

: mid2

MIM:

MIM:300928 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 101; XLID101

MIM:300928 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 101; XLID101

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)