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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:Corneal dystrophy
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Accession:HP:0001131 term browser browse the term
Definition:The term corneal dystrophy embraces a heterogenous group of bilateral genetically determined non-inflammatory corneal diseases that are restricted to the cornea.
Synonyms:alt_id: HP:0007775;   HP:0008005
 xref: SNOMEDCT_US:5587004;   UMLS:C0010036



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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 the eye 0
        Abnormal eye morphology 0
          Abnormal anterior eye segment morphology 0
            Abnormal cornea morphology 0
              Corneal dystrophy 0
                Band-shaped corneal dystrophy 0
                Granular corneal dystrophy 0
                Lattice corneal dystrophy 0
                Marginal corneal dystrophy 0
                Mosaic corneal dystrophy + 0
                Punctate corneal dystrophy 0
                Speckled corneal dystrophy 0
paths to the root