EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 7

General Information (adopted from Orphanet):

Synonyms, Signs: EIG7 MYOCLONIC EPILEPSY, JUVENILE, 2, INCLUDED
EJM2, INCLUDED
Number of Symptoms 4
OrphanetNr:
OMIM Id: 604827
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

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

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0001336) Myoclonus 115 / 7739
2
(HPO:0002069) Generalized tonic-clonic seizures 96 / 7739
3
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739
4
(OMIM) See juvenile myoclonic epilepsy (606904) 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: