Disease #04298 (EIG (epilepsy, idiopathic, generalized (EIG)))

Official abbreviation EIG
Name epilepsy, idiopathic, generalized (EIG)
OMIM ID -
Inheritance -
Individuals reported having this disease 11
Phenotype entries for this disease 11
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2015-07-15 15:03:52 +02:00 (CEST)
Date last edited N/A


Individuals

11 entries on 1 page. Showing entries 1 - 11.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00046513 - PubMed: Chen 2013, Journal: Chen 2013 2-generation family, only child of healthy, unrelated parents F no Italy - >26y - - - EIG see paper; neurologic phenotype of generalized pharmacoresistant epilepsy with mixed seizure types, mild myotonic features, ... CLCN1, CLCN2, CLCN3, CLCN4, CLCN5, CLCN6, CLCN7, CLCNKA CLCN1, CLCNKA 3 1 Johan den Dunnen
00056405 - PubMed: Soldovieri 2014, Journal: Soldovieri 2014 - F no France white - - yes - EIG - - RORB 1 4 Gaetan Lesca
00074466 - PubMed: Lachance-Touchette 2011, Journal: Lachance-Touchette 2011 - - no (Canada) white - - - - EIG Four affected family members over two generations with idiopathic generalizedepilepsy. GABRA1 GABRA1 1 4 Bernt Popp
00074467 - PubMed: Lachance-Touchette 2011, Journal: Lachance-Touchette 2011 - - no Canada white - - - - EIG Four affected individuals over two generations with idiopathic generalizedepilepsy. GABRA1 GABRA1 1 4 Bernt Popp
00074468 - PubMed: Klassen 2011, Journal: Klassen 2011 - ? - - - - - - - EIG Individual with sporadic idiopathic epilepsy not further described. GABRA1 GABRA1 1 1 Bernt Popp
00132051 - - - F - Netherlands - - - - - EIG Generalized myoclonic seizures (HP:0002123), Absence seizures (HP:0002121) KCNMA1 KCNMA1 1 1 Qing Kenneth Wang
00229581 Fam2 - - M no New Zealand - - - Y - autism, EIG, ID Epilepsy, significant intellectual disability with non-verbal autism spectrum disorder (ASD), challenging behaviours. - ARX 1 6 Marie Shaw
00326801 - - - M no China - - - - - EIG Epilepsy, intellectual disability and cerebral palsy of spasticity - CASK 1 2 Tao Cai
00411270 LR17-519 PubMed: Wei 2022 - F - United States African-American - - - - EIG Staring spells; Centrotemporal spikes, BECTS-like. KCNQ5 KCNQ5 1 1 Aguan Daniel Wei
00411272 LR16-508 PubMed: Wei 2022 - M - Netherlands Europe-W - - - - EIG Mild/moderate neurodevelopmental delay. Moderate intellectual disability (FSIQ 50) KCNQ5 KCNQ5 1 1 Aguan Daniel Wei
00436389 - - - M no Italy - - - - - EIG, NDD At the age of 13 months, he had generalized seizure during hyperpyrexia. Eleven more episodes in subsequent years. EEG studies in asleep and awake and head MRI were normal. No further seizures reported after introduction of valproate. GRIN2A GRIN2A 1 1 Pietro Palumbo
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.