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HUMAN PHENOTYPE - ANNOTATIONS

The Human Phenotype Ontology (HPO) is downloaded weekly from http://compbio.charite.de/hudson/job/hpo/lastStableBuild/artifact/ontology/release/hp.obo. The file downloaded is considered the "last stable build" available for the ontology. For more about the HPO, view their website at http://www.human-phenotype-ontology.org/.

Term:Transient myeloproliferative syndrome
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Accession:HP:0005534 term browser browse the term
Definition:A unique clonal neoplastic disorder that is linked to trisomy 21, is restricted to neonatal period, and spontaneously regresses. It often has characteristics of megakaryocytic lineage and is associated with GATA1 mutations in myeloblasts.
Synonyms:exact_synonym: TMD;   Transient leukaemia of Down syndrome;   Transient leukemia of Down syndrome;   Transient myeloproliferative disorder
 xref: SNOMEDCT_US:450934005;   UMLS:C1834582



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Term paths to the root
Path 1
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of blood and blood-forming tissues 0
        Abnormal leukocyte morphology 0
          Leukemia 0
            Myeloproliferative disorder 0
              Transient myeloproliferative syndrome 0
Path 2
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the immune system 0
        Abnormal immune system morphology 0
          Abnormal cellular immune system morphology 0
            Abnormal leukocyte morphology 0
              Leukemia 0
                Myeloproliferative disorder 0
                  Transient myeloproliferative syndrome 0
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