Benign occipital epilepsy

General Information (adopted from Orphanet):

Synonyms, Signs: BOE
Number of Symptoms 5
OrphanetNr: 25968
OMIM Id: 132090
ICD-10: G40.0
UMLs: C1851549
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Childhood-onset epilepsy syndrome
 -Rare genetic disease
 -Rare neurologic disease

Symptom Information: Sort by abundance 

1
 (HPO:0002353) EEG abnormality 188 / 7739
2
 (HPO:0001250) Seizures 1245 / 7739
3
 (OMIM) Typical EEG abnormality 1 / 7739
4
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739
5
 (OMIM) Benign occipital epilepsy 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: