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Amyotrophic lateral sclerosis-parkinsonism-dementia complex
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Lennox-Gastaut syndrome
3 associated genes
No signs/symptoms info
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Lennox-Gastaut syndrome

PARK7
(UniProt - OMIM)
 CHD2
(UniProt - OMIM)
TRPM7
(UniProt - OMIM)
 MAPK10
(UniProt - OMIM)
SCN1A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PARK7
(0.63)
CHD2


Citations in the biomedical literature:


Amyotrophic lateral sclerosis-parkinsonism-dementia complex
PARK7 TRPM7
Lennox-Gastaut syndrome
CHD2 MAPK10 SCN1A



Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Lennox-Gastaut syndrome

Synonym(s):
- Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam
- Guam disease
- Lytico-Bodig disease
- PDALS
- Parkinsonism-dementia-ALS complex
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
1 MeSH reference: C535500
No signs/symptoms info available.