syndromic X-linked intellectual disability Raymond type

Summary

DOID:0060824 - syndromic X-linked intellectual disability Raymond type

Disease Ontology Definition:A syndromic X-linked intellectual disability characterized by intellectual disability and marfanoid habitus that has_material_basis_in mutation in the ZDHHC9 gene on chromosome Xq26.1.

Synonyms: MRXSR, X-linked syndromic intellectual developmental disorder Raymond type, mental retardation, X-linked syndromic, Raymond type,

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

: zdhhc9

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010427 - syndromic X-linked intellectual disability Raymond type

MONDO:0010427 - syndromic X-linked intellectual disability Raymond type

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): syndromic X-linked intellectual disability (is_a)