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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:Petty Laxova Wiedemann Syndrome
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Accession:DOID:9001903 term browser browse the term
Synonyms:primary_id: MESH:C537886

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14196
    syndrome 9376
      Petty Laxova Wiedemann Syndrome 0
Path 2
Term Annotations click to browse term
  disease 14196
    Developmental Disease 12386
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 11617
        genetic disease 11308
          monogenic disease 9486
            autosomal genetic disease 8807
              autosomal dominant disease 5808
                progeria 19
                  Petty Laxova Wiedemann Syndrome 0
paths to the root