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.
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
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