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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:Absence of Septum Pellucidum
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Accession:DOID:9001023 term browser browse the term
Synonyms:primary_id: MESH:C535562;   RDO:0000757

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16063
    syndrome 9327
      septooptic dysplasia 16
        Absence of Septum Pellucidum 0
Path 2
Term Annotations click to browse term
  disease 16063
    Developmental Disease 15996
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 15949
        genetic disease 15939
          monogenic disease 9437
            autosomal genetic disease 8755
              septooptic dysplasia 16
                Absence of Septum Pellucidum 0
paths to the root