Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the skin (HP:0000951)help
Grandparent Node:
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Neoplasm by anatomical site (HP:0011793)help
Parent Node:
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Neoplasm of the skin (HP:0008069)help
..Starting node
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Seborrheic keratosis (HP:0031287)help
Term ID: 31287
Name: Seborrheic keratosis
Synonym: Basal cell papilloma; Seborrheic verruca; Senile wart
Definition: A raised growth on the skin of older individuals. The lesion usually is initially light tan and may darken to dark brown or nearly black. The consistent feature of seborrheic keratoses is their waxy, pasted-on or stuck-on look.
Comments:
Reference: HP:0031287
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcanthoma (HP:0025432) help
..expandActinic keratosis (HP:0025127) help
..expandAdenoma sebaceum (HP:0009720) help
..expandBasal cell carcinoma (HP:0002671) help
..expandCutaneous angiolipomas (HP:0006773) help
..expandCutaneous leiomyoma (HP:0007620) help
..expandCutaneous leiomyosarcoma (HP:0006755) help
..expandCutaneous mastocytosis (HP:0200151) help
..expandCutaneous melanoma (HP:0012056) help
..expandCutaneous myxoma (HP:0030428) help
..expandEccrine syringofibroadenoma (HP:0031018) help
..expandFibrofolliculoma (HP:0030436) help
..expandFrontal cutaneous lipoma (HP:0007541) help
..expandKaposi's sarcoma (HP:0100726) help
..expandKeratoacanthoma (HP:0031525) help
..expandLymphocytoma cutis (HP:0031549) help
..expandMerkel cell skin cancer (HP:0030447) help
..expandMultiple cutaneous leiomyomas (HP:0007437) help
..expandMultiple cutaneous malignancies (HP:0007606) help
..expandMyxoid subcutaneous tumors (HP:0006769) help
..expandNeurofibromas (HP:0001067) help
..expandPapilloma (HP:0012740) help
..expandPeripheral Schwannoma (HP:0009593) help
..expandSkin appendage neoplasm (HP:0012842) help
..expandSquamous cell carcinoma (HP:0002860) help
..expandSteatocystoma multiplex (HP:0012035) help
..expandSubcutaneous lipoma (HP:0001031) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0031287HP:0031287Seborrheic keratosis0ERCC4 CL E G H2072278760Xeroderma pigmentosum, group F278760C0268140OMIM15383436133520
HP:0031287HP:0031287Seborrheic keratosis0ERCC4 CL E G H2072278760Xeroderma pigmentosum, group F278760C0268140OMIM14693436133520
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031287HP:0031287Seborrheic keratosis0NTHL1 CL E G H4913454840ORPHA09028028602656
HP:0031287HP:0031287Seborrheic keratosis0NTHL1 CL E G H4913454840ORPHA07558028602656


Genes (2) :ERCC4 NTHL1

Diseases (2) :278760 454840
 

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