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DOID:0111844 - X-linked intellectual developmental disorder 108
Disease Ontology Definition:A syndromic X-linked intellectual disability characterized by global developmental delay, delayed walking, and poor speech acquisition that has_material_basis_in hemizygous mutation in the SLC9A7 gene on chromosome Xp11.3.
Synonyms: MRX108,
Xenbase Genes :
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),
syndromic X-linked intellectual disability (is_a)