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Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome

PIK3CA
(UniProt - OMIM)
 ATR
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PIK3CA
(0.63)
ATR


Citations in the biomedical literature:


Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
PIK3CA
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
ATR



Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
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: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.