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RGD uses the Human Disease Ontology (DO, 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:familial chronic myelocytic leukemia-like syndrome
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Accession:DOID:0060761 term browser browse the term
Definition:A chronic myeloid leukemia characterized by chronic myelocytic leukemia in early infancy and absence of the BCR/ABL fusion gene (Philadelphia chromosome). (DO)
Synonyms:exact_synonym: Cml-Like Syndrome, Familial
 primary_id: MESH:C536093;   RDO:0001524
 alt_id: OMIM:600080
For additional species annotation, visit the Alliance of Genome Resources.

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familial chronic myelocytic leukemia-like syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Irf8 interferon regulatory factor 8 ISS OMIM:600080 MouseDO NCBI chr19:54,314,859...54,336,643
Ensembl chr19:54,314,865...54,336,640
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17126
    disease of cellular proliferation 6943
      Hereditary Neoplastic Syndromes 912
        familial chronic myelocytic leukemia-like syndrome 1
Path 2
Term Annotations click to browse term
  disease 17126
    disease of anatomical entity 16474
      Hemic and Lymphatic Diseases 2217
        hematopoietic system disease 1797
          Hematologic Neoplasms 854
            Bone Marrow Neoplasms 353
              bone marrow cancer 353
                myeloid neoplasm 291
                  chronic myeloid leukemia 86
                    familial chronic myelocytic leukemia-like syndrome 1
paths to the root