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RGD uses the Human Disease Ontology (DO, 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:developmental and epileptic encephalopathy 90
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Accession:DOID:0070381 term browser browse the term
Definition:A developmental and epileptic encephalopathy characterized by onset of refractory seizures in the first days or months of life that has_material_basis_in hemizygous or heterozygous mutation in the FGF13 gene on chromosome Xq26. (DO)
Synonyms:exact_synonym: DEE90
 primary_id: OMIM:301058
 alt_id: DOID:9000663

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developmental and epileptic encephalopathy 90 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Fgf13 fibroblast growth factor 13 ISO ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 90 OMIM
PMID:25741868 PMID:33245860 PMID:34871784 NCBI chr  X:137,276,498...137,800,056
Ensembl chr  X:137,276,511...137,800,391
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21142
    syndrome 10749
      electroclinical syndrome 1351
        developmental and epileptic encephalopathy 977
          developmental and epileptic encephalopathy 90 1
Path 2
Term Annotations click to browse term
  disease 21142
    disease of anatomical entity 18190
      nervous system disease 14019
        central nervous system disease 12373
          brain disease 11610
            epilepsy 2798
              electroclinical syndrome 1351
                neonatal period electroclinical syndrome 951
                  early infantile epileptic encephalopathy 931
                    developmental and epileptic encephalopathy 90 1
paths to the root