Photosensitive epilepsy

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 3
OrphanetNr: 166409
OMIM Id: 132100
226800
ICD-10: G40.8
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Reflex epilepsy
 -Rare genetic disease
 -Rare neurologic disease

Symptom Information: Sort by abundance 

1
 (HPO:0010852) EEG with photoparoxysmal response 7 / 7739
2
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739
3
 (HPO:0003831) Age-dependent penetrance 4 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: