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The Human Phenotype Ontology (HPO) is downloaded weekly from The file downloaded is considered the "last stable build" available for the ontology. For more about the HPO, view their website at

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