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DO Term : speech-language disorder-1 [DOID:0111275] Disease Ontology

Namespace

disease_ontology

Obsolete

false

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.

synonyms:
GARD:12889,
developmental verbal dyspraxia,
ORDO:209908,
602081,
CAS,
speech and language disorder with orofacial dyspraxia,
speech-language disorder type 1,
developmental apraxia of speech,
childhood apraxia of speech,
OMIM:602081,
articulatory apraxia

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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