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Epilepsy with myoclonic-astatic seizures
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
1 OMIM reference -
2 associated genes
No signs/symptoms info
Epilepsy with myoclonic-astatic seizures
Amyotrophic lateral sclerosis-parkinsonism-dementia complex

CHD2
(UniProt - OMIM)
 PARK7
(UniProt - OMIM)
SCN1A
(UniProt - OMIM)
 TRPM7
(UniProt - OMIM)
SLC2A1
(UniProt - OMIM)

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


Citations in the biomedical literature:


Epilepsy with myoclonic-astatic seizures
CHD2 SCN1A SLC2A1
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
PARK7 TRPM7



Epilepsy with myoclonic-astatic seizures
Amyotrophic lateral sclerosis-parkinsonism-dementia complex

Synonym(s):
- Doose syndrome
- EMAS
- Epilepsy with myoclonic-atonic seizures
- MAE
- Myoclonic atonic epilepsy
- Myoclonic-astatic epilepsy in early childhood
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 neurologic disease
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: unknown
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.