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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:Color vision defect
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Accession:HP:0000551 term browser browse the term
Definition:An anomaly in the ability to discriminate between or recognize colors.
Synonyms:exact_synonym: Abnormal color vision;   Abnormal colour vision;   Abnormality of color vision;   Abnormality of colour vision;   Disturbed color vision;   Disturbed colour vision
 related_synonym: COLOR VISION DEFECT, SEVERE;   COLOR VISION DEFECTS;   Colour vision defect;   Colour vision defect, severe;   Colour vision defects;   Loss in color vision;   Loss in colour vision
 xref: SNOMEDCT_US:23289000;   SNOMEDCT_US:367469000;   UMLS:C0009398;   UMLS:C0234629;   UMLS:C3552853


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Path 1
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the eye 0
        Abnormal eye physiology 0
          Abnormality of vision 0
            Color vision defect 0
              Color vision test abnormality + 0
              Dyschromatopsia + 0
              Monochromacy + 0
paths to the root