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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:Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay
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Accession:DOID:9001356 term browser browse the term
Synonyms:primary_id: MESH:C563345
 alt_id: MIM:601347


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19102
    syndrome 11271
      myelodysplastic syndrome 243
        Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay 0
Path 2
Term Annotations click to browse term
  disease 19102
    disease of anatomical entity 18443
      Hemic and Lymphatic Diseases 4331
        hematopoietic system disease 3821
          bone marrow disease 839
            Bone Marrow Neoplasms 510
              bone marrow cancer 510
                myelodysplastic syndrome 243
                  Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay 0
paths to the root