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Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 3
Autoimmune lymphoproliferative syndrome
3 OMIM references -
5 associated genes
No signs/symptoms info
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Autoimmune lymphoproliferative syndrome

PIK3CA
(UniProt - OMIM)
 CASP10
(UniProt - OMIM)
FAS
(UniProt - OMIM)
FASLG
(UniProt - OMIM)
NRAS
(UniProt - OMIM)
PRKCD
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PIK3CA
PIK3CA
PIK3CA
(0.71)
(0.52)
(0.49)
NRAS
PRKCD
FASLG


Citations in the biomedical literature:


Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
PIK3CA
Autoimmune lymphoproliferative syndrome
CASP10 FAS FASLG NRAS PRKCD



Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Autoimmune lymphoproliferative syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- ALPS
- Canale-Smith syndrome
- FAS deficiency
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare immune disease
- Rare oncologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: D056735
No signs/symptoms info available.