non-syndromic X-linked intellectual disability 106

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Summary

Literature (0)

DOID:0080240 - non-syndromic X-linked intellectual disability 106

Disease Ontology Definition:A non-syndromic X-linked intellectual disability that has_material_basis_in hemizygous mutation in OGT on chromosome Xq13.1.

Synonyms: MRX106, X-linked mental retardation 106

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

: ogt

MIM:

MIM:300997 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 106; XLID106

MIM:300997 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 106; XLID106

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)