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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:Clinical modifier
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Accession:HP:0012823 term browser browse the term
Definition:This subontology is designed to provide terms to characterize and specify the phenotypic abnormalities defined in the Phenotypic abnormality subontology, with respect to severity, laterality, age of onset, and other aspects.
Comment:Note that some of the terms, such as Intellectual disability, have children terms such as Severe intellectual disability that represent precomposed combinations of modifiers and phenotypic abnormality terms. This done where the medical community commonly uses these terms with a fixed meaning (for instance, the Intellectual disability terms are used with specific IQ ranges). For computational reasoning, the semantics are intended to be the same as if there was a combination of the phenotype term and the clinical modifier term.
Synonyms:exact_synonym: Phenotypic modifier
 alt_id: HP:0000004
 xref: UMLS:C4021064



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Term paths to the root
Path 1
Term Annotations click to browse term
  Human phenotype 0
    Clinical modifier 0
      Aggravated by + 0
      Ameliorated by + 0
      Clinical course + 0
      Clinical relevance + 0
      Fluctuance on palpation 0
      Fracture type + 0
      Pain characteristic + 0
      Phenotypic variability + 0
      Position + 0
      Refractory 0
      Severity + 0
      Triggered by + 0
      Worse in evening 0
paths to the root