Reading seizures

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 7
OrphanetNr: 166433
OMIM Id: 132300
ICD-10: G40.8
UMLs:
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: Reflex epilepsy
 -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
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739
4
 (OMIM) Reading epilepsy 1 / 7739
5
 (HPO:0003621) Juvenile onset 105 / 7739
6
 (OMIM) Seizures related to pattern and photosensitivity 1 / 7739
7
 (OMIM) EEG discharges during reading 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: