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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:Myelodysplasia
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Accession:HP:0002863 term browser browse the term
Definition:Clonal hematopoietic stem cell disorders characterized by dysplasia (ineffective production) in one or more hematopoietic cell lineages, leading to anemia and cytopenia.
Synonyms:exact_synonym: Myelodysplastic syndrome
 related_synonym: Hypoplastic myelodysplasia
 alt_id: HP:0004832;   HP:0006730
 xref: EFO:0000198;   SNOMEDCT_US:109995007;   SNOMEDCT_US:128623006;   SNOMEDCT_US:188736006;   UMLS:C1851971;   UMLS:C3463824


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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
        Hematological neoplasm 0
          Myelodysplasia 0
            Bilineage myelodysplasia 0
            Multiple lineage myelodysplasia 0
            Single lineage myelodysplasia + 0
Path 2
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Neoplasm 0
        Neoplasm by anatomical site 0
          Hematological neoplasm 0
            Myelodysplasia 0
              Bilineage myelodysplasia 0
              Multiple lineage myelodysplasia 0
              Single lineage myelodysplasia + 0
paths to the root