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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 4
3 OMIM references -
5 associated genes
No signs/symptoms info
Intermittent hydrarthrosis
Autoimmune lymphoproliferative syndrome

MEFV CASP10
TNFRSF1A FAS
FASLG
NRAS
PRKCD


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TNFRSF1A
TNFRSF1A
TNFRSF1A
TNFRSF1A
(0.86)
(0.77)
(0.65)
(0.55)
CASP10
FASLG
PRKCD
FAS



Citations in the biomedical literature:


Intermittent hydrarthrosis
MEFV TNFRSF1A
Autoimmune lymphoproliferative syndrome
CASP10 FAS FASLG NRAS PRKCD



Intermittent hydrarthrosis
Autoimmune lymphoproliferative syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- ALPS
- Canale-Smith syndrome
- FAS deficiency

Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic 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.