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1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
5 OMIM references -
2 associated genes
8 signs/symptoms
Cree leukoencephalopathy
Benign adult familial myoclonic epilepsy

EIF2B1 ADRA2B
EIF2B2 CNTN2
EIF2B3
EIF2B4
EIF2B5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EIF2B1
(0.83)
ADRA2B



Citations in the biomedical literature:


Cree leukoencephalopathy
EIF2B1 EIF2B2 EIF2B3 EIF2B4 EIF2B5
Benign adult familial myoclonic epilepsy
ADRA2B CNTN2



Cree leukoencephalopathy
Benign adult familial myoclonic epilepsy

Synonym(s):
(no synonyms)

Synonym(s):
- ADCME
- Autosomal dominant cortical myoclonus and epilepsy
- BAFME
- FAME
- FCMTE
- Familial adult myoclonic epilepsy
- Familial cortical myoclonic tremor and epilepsy

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

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: elderly
Type of inheritance: autosomal dominant

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

Benign adult familial myoclonic epilepsy

Very frequent
- Autosomal dominant inheritance
- EEG anomalies
- Myoclonus / fasciculations
- Tremor

Frequent
- Seizures / epilepsy / absences / spasms / status epilepticus

Occasional
- Facial pain / cephalalgia / migraine
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Transient amaurosis / acute visual trouble


Cree leukoencephalopathy

(no data available)