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

MONDO:0010427 - ciliary processes

MIM:

MIM:300799 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR

MIM:300799 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR

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

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

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