autosomal dominant intellectual developmental disorder 39

Summary

DOID:0070069 - autosomal dominant intellectual developmental disorder 39

Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant heterozygous mutation in the MYT1L gene on chromosome 2p25.3.

Synonyms: autosomal dominant mental retardation 39, autosomal dominant non-syndromic intellectual disability 39, MRD39

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

: myt1l

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014678 - intellectual disability, autosomal dominant 39

MONDO:0014678 - intellectual disability, autosomal dominant 39

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

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

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