autosomal dominant non-syndromic intellectual disability 1

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Echinobase

Summary

Literature (0)

DOID:0070031 - autosomal dominant non-syndromic intellectual disability 1

Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of MBD5 on chromosome 2q23.1.

Synonyms: MRD1, autosomal dominant mental retardation 1,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

OMIM:

MIM:156200 - mental retardation, autosomal dominant 1; mrd1 chromosome 2q23.1 deletion syndrome, included

MIM:156200 - mental retardation, autosomal dominant 1; mrd1 chromosome 2q23.1 deletion syndrome, included

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

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

Parent(s): autosomal dominant intellectual developmental disorder (is_a)