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Childhood apraxia of speech
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
7q31 microdeletion syndrome
Intellectual disability-severe speech delay-mild dysmorphism syndrome
MALT lymphoma
Precursor B-cell acute lymphoblastic leukemia
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
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
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
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
FOXP2 O15409605317
No signs/symptoms info available.