syndromic intellectual disability

Summary

DOID:0050888 - syndromic intellectual disability

Disease Ontology Definition:An intellectual disability that is characterized by the presence of associated medical and behavioral sign and symptoms.

Synonyms:

Echinobase 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

: LOC585120, LOC762707, cask, atp6ap2, pqbp1, hsd17b10, phf8, igbp1

MIM:

MIM:300486 - mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance
MIM:300860 - mental retardation, x-linked, syndromic, nascimento type; mrxsn
MIM:309583 - mental retardation, x-linked, syndromic, snyder-robinson type; mrxssr

MIM:300486 - mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance

MIM:300860 - mental retardation, x-linked, syndromic, nascimento type; mrxsn

MIM:309583 - mental retardation, x-linked, syndromic, snyder-robinson type; mrxssr

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

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

Parent(s): intellectual disability (is_a)