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Intellectual disability-severe speech delay-mild dysmorphism syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
7q31 microdeletion syndrome
1 associated gene
No signs/symptoms info
Intellectual disability-severe speech delay-mild dysmorphism syndrome
7q31 microdeletion syndrome

FOXP1
(UniProt - OMIM)
 FOXP2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FOXP1
(0.81)
FOXP2


Citations in the biomedical literature:


Intellectual disability-severe speech delay-mild dysmorphism syndrome
FOXP1
7q31 microdeletion syndrome
FOXP2



Intellectual disability-severe speech delay-mild dysmorphism syndrome
7q31 microdeletion syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Del(7)(q31)
- Monosomy 7q31
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):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.