non-syndromic X-linked intellectual disability 99

Summary

DOID:0112026 - non-syndromic X-linked intellectual disability 99

Disease Ontology Definition:A non-syndromic X-linked intellectual disability characterized by developmental delay, hypotonia, and variable behavioral abnormalities that has_material_basis_in hemizygous mutation in the USP9X gene on chromosome Xp11.4.

Synonyms: MRX99, X-linked mental retardation 99

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

: usp9x

MIM:

MIM:300919 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99; XLID99

MIM:300919 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99; XLID99

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)