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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Autoimmune lymphoproliferative syndrome with recurrent infections
Amyotrophic lateral sclerosis-parkinsonism-dementia complex

CASP8 PARK7
TRPM7


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CASP8
(0.56)
PARK7



Citations in the biomedical literature:


Autoimmune lymphoproliferative syndrome with recurrent infections
CASP8
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
PARK7 TRPM7



Autoimmune lymphoproliferative syndrome with recurrent infections
Amyotrophic lateral sclerosis-parkinsonism-dementia complex

Synonym(s):
- ALPS with recurrent infections

Synonym(s):
- Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam
- Guam disease
- Lytico-Bodig disease
- PDALS
- Parkinsonism-dementia-ALS complex

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

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

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

No signs/symptoms info available.