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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: CAS, articulatory apraxia, 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](img/icons/info1.png)
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee