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 USP9X 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

: usp9x

OMIM:

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

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

Other Model Organisms: AGR, 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)