ZFIN Human Disease: speech-language disorder-1

OBO ID: DOID:0111275

Term Name:	speech-language disorder-1		Search Ontology:
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
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. (2)
References:	GARD:12889 OMIM:602081 ORDO:209908
Ontology:	Human Disease ( DOID:0111275 )

Relationships

is a type of:	autosomal dominant disease speech disorder autosomal dominant disease speech disorder Show first 5 Terms

OTHER speech-language disorder-1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
FOXP2	foxp2	Speech-language disorder-1	602081

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None