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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Autoimmune lymphoproliferative syndrome with recurrent infections
Familial retinoblastoma

CASP8 RB1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CASP8
(0.55)
RB1



Citations in the biomedical literature:


Autoimmune lymphoproliferative syndrome with recurrent infections
CASP8
Familial retinoblastoma
RB1



Autoimmune lymphoproliferative syndrome with recurrent infections
Familial retinoblastoma

Synonym(s):
- ALPS with recurrent infections

Synonym(s):
- Bilateral retinoblastoma
- Hereditary retinoblastoma

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare oncologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.