| Metadata | |
|---|---|
| ID | DOID:0111275 |
| Name | speech-language disorder-1 |
| 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. https://www.ncbi.nlm.nih.gov/pubmed/11586359, https://www.ncbi.nlm.nih.gov/pubmed/1934976 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
articulatory apraxia [EXACT] CAS [EXACT] childhood apraxia of speech [EXACT] developmental apraxia of speech [EXACT] developmental verbal dyspraxia [EXACT] speech and language disorder with orofacial dyspraxia [EXACT] speech-language disorder type 1 [EXACT] |
| Parent Relationships |
is_a autosomal dominant disease is_a speech disorder |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |