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

CASP10
(UniProt - OMIM)
 PIK3CA
(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)
NRAS
PRKCD
FASLG
(0.71)
(0.52)
(0.49)
PIK3CA
PIK3CA
PIK3CA


Citations in the biomedical literature:


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



Autoimmune lymphoproliferative syndrome
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia

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