Human Phenotype Ontology 
Grandparent Node:
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Localized skin lesion (HP:0011355)help
Parent Node:
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Hyperkeratosis (HP:0000962)help
Parent Node:
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Papule (HP:0200034)help
..Starting node
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Hyperkeratotic papule (HP:0045059)help
Term ID: 45059
Name: Hyperkeratotic papule
Synonym:
Definition: A circumscribed, solid elevation of skin with no visible fluid, varying in size from a pinhead to less than 10mm in diameter at the widest point that is composed of localized hyperkeratosis (the latter may be demonstrated histopathologically).
Comments:
Reference: HP:0045059
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandErythematous papule (HP:0030350) help
..expandGottron's papules (HP:0025508) help
..expandHyperpigmented papule (HP:0025473) help
..expandIntermittent generalized erythematous papular rash (HP:0007432) help
..expandPiezogenic pedal papules (HP:0025509) help
..expandSkin-colored papule (HP:0025512) help
..expandVerrucous papule (HP:0012500) help
..expandWhite papule (HP:0031289) help
..expandYellow papule (HP:0025507) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0045059HP:0045059Hyperkeratotic papule0POFUT1 CL E G H23509615327Dowling-Degos disease 2615327C3809147OMIM05214988607491
HP:0045059HP:0045059Hyperkeratotic papule0POFUT1 CL E G H23509615327Dowling-Degos disease 2615327C3809147OMIM05814988607491


Genes (1) :POFUT1

Diseases (1) :615327
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.