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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:Focal Cortical Dysplasia of Taylor, Type IIA
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Accession:DOID:9004903 term browser browse the term
Synonyms:exact_synonym: CDTD;   Cortical Dysplasia of Taylor without Balloon Cells;   Cortical Dysplasia of Taylor, Dysplasia Only;   FCD IIA;   FCD2A;   FCORD2A;   FOCAL CORTICAL DYSPLASIA, TYPE IIA
 primary_id: MESH:C564583
For additional species annotation, visit the Alliance of Genome Resources.


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16158
    disease of anatomical entity 15408
      nervous system disease 11007
        central nervous system disease 9126
          brain disease 8438
            epilepsy 1505
              Focal Cortical Dysplasia of Taylor 5
                Focal Cortical Dysplasia of Taylor, Type IIA 0
Path 2
Term Annotations click to browse term
  disease 16158
    Developmental Disease 9628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8455
        genetic disease 7972
          monogenic disease 5749
            autosomal genetic disease 4887
              autosomal dominant disease 3117
                complex cortical dysplasia with other brain malformations 717
                  Malformations of Cortical Development, Group I 575
                    Focal Cortical Dysplasia of Taylor 5
                      Focal Cortical Dysplasia of Taylor, Type IIA 0
paths to the root