ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Childhood apraxia of speech

Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FOXP2	(0.63)	GATAD2B

Citations in the biomedical literature:

Childhood apraxia of speech		Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
	Synonym(s): - CAS - Developmental verbal dyspraxia - Speech and language disorder with orofacial dyspraxia - Speech-language disorder type 1		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): (no data available)		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.