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Summary Literature (0)
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 : usp9x


OMIM:
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)