Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:generalized epilepsy with febrile seizures plus 2
go back to main search page
Accession:DOID:0111294 term browser browse the term
Definition:A generalized epilepsy with febrile seizures plus that has_material_basis_in heterozygous mutation in SCN1A on chromosome 2q24.3. (DO)
Synonyms:exact_synonym: GEFS+, type 2;   GEFS+2;   GEFSP2;   generalised epilepsy with febrile seizures plus 2;   generalised epilepsy with febrile seizures plus type 2;   generalized epilepsy with febrile seizures plus, type 2
 narrow_synonym: FEB3A;   GEFS+2 familial febrile seizures 3A
 primary_id: MESH:C565810
 alt_id: MIM:604403



show annotations for term's descendants           Sort by:
generalized epilepsy with febrile seizures plus 2 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Reln reelin ISO ClinVar Annotator: match by term: Generalized epilepsy with febrile seizures plus, type 2 ClinVar PMID:25741868 PMID:28492532 NCBI chr 4:12,736,177...13,162,956
Ensembl chr 4:12,736,130...13,162,211
JBrowse link
G Scn1a sodium voltage-gated channel alpha subunit 1 ISO DNA:missense mutations:cds:p.T875M, p.R1648H (human)
CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: GEFS+, TYPE 2 | ClinVar Annotator: match by term: Generalized epilepsy with febrile seizures plus, type 2
OMIM
CTD
ClinVar
RGD
PMID:1893009 PMID:1893099 PMID:9126059 PMID:9536098 PMID:10486327 More... RGD:727292 NCBI chr 3:50,952,790...51,071,804
Ensembl chr 3:50,952,791...51,071,699
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19106
    disease of anatomical entity 18445
      nervous system disease 14349
        central nervous system disease 12613
          brain disease 11840
            epilepsy 2996
              Febrile Seizures 61
                generalized epilepsy with febrile seizures plus 28
                  generalized epilepsy with febrile seizures plus 2 2
Path 2
Term Annotations click to browse term
  disease 19106
    disease of anatomical entity 18445
      nervous system disease 14349
        central nervous system disease 12613
          brain disease 11840
            epilepsy 2996
              Generalized Epilepsy 470
                idiopathic generalized epilepsy 307
                  generalized epilepsy with febrile seizures plus 28
                    generalized epilepsy with febrile seizures plus 2 2
paths to the root