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Disease Ontology Browser
speech-language disorder-1 (DOID:0111275)
Alliance: disease page
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
Alt IDs: OMIM:602081, ORDO:209908
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory