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

PARK7
(UniProt - OMIM)
 CASP8
(UniProt - OMIM)
TRPM7
(UniProt - OMIM)

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


Citations in the biomedical literature:


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



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

Synonym(s):
- Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam
- Guam disease
- Lytico-Bodig disease
- PDALS
- Parkinsonism-dementia-ALS complex
Synonym(s):
- ALPS with recurrent infections
Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the nervous system -
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: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.