speech-language disorder-1

Summary
Synonym
  • 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
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.
Super Class
autosomal dominant disease speech disorder
Disease Ontology
DOID:0111275
Mondo Disease Ontology
ORDO
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
93986 FOXP2 forkhead box P2
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
O15409 Forkhead box protein P2

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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