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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:Hyperparakeratosis
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Accession:HP:0040009 term browser browse the term
Definition:Abnormal keratinization of the epidermal stratum coreum (horny layer) with increased keratin formation, preservation of the nuclei in the superficial cells, and absence of the stratum granulosum.
Synonyms:xref: SNOMEDCT_US:125554003;   UMLS:C1265968


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Hyperparakeratosis term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G KRT10 keratin 10 IAGP HPO MIM:607602 NCBI chr17:40,818,117...40,822,614
Ensembl chr17:40,818,117...40,822,614 		JBrowse link
G KRT13 keratin 13 IAGP HPO MIM:615785 NCBI chr17:41,500,981...41,505,612
Ensembl chr17:41,500,981...41,505,705 		JBrowse link
G PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha IAGP HPO ORPHA:276280 NCBI chr 3:179,148,126...179,240,093
Ensembl chr 3:179,148,114...179,240,093 		JBrowse link
G TRPV3 transient receptor potential cation channel subfamily V member 3 IAGP HPO MIM:614594 NCBI chr17:3,510,502...3,557,812
Ensembl chr17:3,510,502...3,557,812 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  Human phenotype 73835
    Phenotypic abnormality 73530
      Abnormality of the integument 6107
        Abnormality of the skin 5435
          Abnormal skin morphology 2573
            Thickened skin 688
              Epidermal thickening 389
                Parakeratosis 33
                  Hyperparakeratosis 4
paths to the root