Speech-Language Disorder-1
Disease ID: disease_node_15862
Connections displayed (default: 10).
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| Dbxref | GARD:12889, MIM:602081, ORDO:209908 |
|---|---|
| Subclassof | DOID_0050736, DOID_92 |
| Data Source | DOID |
| 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 |
| Doid Label | speech-language disorder-1 |
| Doid Description | 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. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_15862 |
| Doid Id | DOID_0111275 |
| Label | Speech-Language Disorder-1 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Speech Disorders(ID:disease_node_7013) (Disease)