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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:Wiskott-Aldrich Syndrome, Autosomal Dominant Form
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Accession:DOID:9003667 term browser browse the term
Synonyms:primary_id: MESH:C563431
 alt_id: OMIM:600903


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 41189
    syndrome 18075
      primary immunodeficiency disease 5019
        lymphopenia 47
          Wiskott-Aldrich syndrome 8
            Wiskott-Aldrich Syndrome, Autosomal Dominant Form 0
Path 2
Term Annotations click to browse term
  disease 41189
    Developmental Disease 36464
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 33606
        genetic disease 33187
          monogenic disease 18511
            X-linked monogenic disease 2088
              X-linked recessive disease 938
                Wiskott-Aldrich syndrome 8
                  Wiskott-Aldrich Syndrome, Autosomal Dominant Form 0
paths to the root