speech-language disorder-1

Summary

DOID:0111275 - speech-language disorder-1

Disease Ontology Definition:A speech disorder characterized by severe orofacial dyspraxia resulting in largely incomprehensible speech that has_material_basis_in heterozygous mutation in FOXP2 on 7q31.1.

Synonyms: articulatory apraxia, CAS, childhood apraxia of speech, developmental apraxia of speech, developmental verbal dyspraxia, speech and language disorder with orofacial dyspraxia, speech-language disorder type 1

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

: foxp2

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

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

Parent(s): autosomal dominant disease (is_a), speech disorder (is_a)