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
..expand
Papilloma (HP:0012740)help
Term ID: 12740
Name: Papilloma
Synonym:
Definition: A tumor of the skin or mucous membrane with finger-like projections.
Comments:
Reference: HP:0012740
Genes and Diseases:
 
       Child Nodes:
........expandSquamous Papilloma (HP:0031021) help
................... HP:0031022 Oropharyngeal squamous papilloma
........expandFacial papilloma (HP:0040167) help
........expandChoroid plexus papilloma (HP:0200022) help
........expandVerrucae (HP:0200043) help
................... HP:0550004 Verruca plana

 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
..expandPeripheral Schwannoma (HP:0009593) help
..expandSeborrheic keratosis (HP:0031287) 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:0012740HP:0012740Papilloma0AKT1 CL E G H207201ORPHA112391164730
HP:0012740HP:0012740Papilloma0DDB2 CL E G H1643910Blepharoptosis aortic anomalyORPHA1172718600811
HP:0012740HP:0012740Papilloma0ERCC2 CL E G H2068910Blepharoptosis aortic anomalyORPHA11083434126340
HP:0012740HP:0012740Papilloma0ERCC3 CL E G H2071910Blepharoptosis aortic anomalyORPHA1203435133510
HP:0012740HP:0012740Papilloma0ERCC4 CL E G H2072910Blepharoptosis aortic anomalyORPHA1723436133520
HP:0012740HP:0012740Papilloma0ERCC5 CL E G H2073910Blepharoptosis aortic anomalyORPHA1593437133530
HP:0012740HP:0012740Papilloma0HRAS CL E G H32653071ORPHA1345173190020
HP:0012740HP:0012740Papilloma0KLLN CL E G H100144748201ORPHA1837212612105
HP:0012740HP:0012740Papilloma0MSH3 CL E G H4437480536ORPHA1277326600887
HP:0012740HP:0012740Papilloma0MSH3 CL E G H4437617100Familial adenomatous polyposis 4617100C4310719OMIM1277326600887
HP:0012740HP:0012740Papilloma0PIK3CA CL E G H5290201ORPHA1578975171834
HP:0012740HP:0012740Papilloma0PORCN CL E G H648402092EhrlichiosisORPHA112117652300651
HP:0012740HP:0012740Papilloma0PTEN CL E G H5728201ORPHA16589588601728
HP:0012740HP:0012740Papilloma0SDHB CL E G H6390201ORPHA127910681185470
HP:0012740HP:0012740Papilloma0SDHC CL E G H6391201ORPHA16210682602413
HP:0012740HP:0012740Papilloma0SDHD CL E G H6392201ORPHA117410683602690
HP:0012740HP:0012740Papilloma0SEC23B CL E G H10483201ORPHA112610702610512
HP:0012740HP:0012740Papilloma0SEC23B CL E G H10483616858616858616858OMIM112610702610512
HP:0012740HP:0012740Papilloma0XPA CL E G H7507910Blepharoptosis aortic anomalyORPHA15112814611153
HP:0012740HP:0012740Papilloma0XPC CL E G H7508910Blepharoptosis aortic anomalyORPHA110012816613208
HP:0012740HP:0012740Papilloma1AKT1 CL E G H207201ORPHA112391164730
HP:0012740HP:0012740Papilloma1DDB2 CL E G H1643910Blepharoptosis aortic anomalyORPHA1172718600811
HP:0012740HP:0012740Papilloma1ERCC2 CL E G H2068910Blepharoptosis aortic anomalyORPHA11083434126340
HP:0012740HP:0012740Papilloma1ERCC3 CL E G H2071910Blepharoptosis aortic anomalyORPHA1203435133510
HP:0012740HP:0012740Papilloma1ERCC4 CL E G H2072910Blepharoptosis aortic anomalyORPHA1723436133520
HP:0012740HP:0012740Papilloma1ERCC5 CL E G H2073910Blepharoptosis aortic anomalyORPHA1593437133530
HP:0012740HP:0012740Papilloma1HRAS CL E G H32653071ORPHA1345173190020
HP:0012740HP:0012740Papilloma1KLLN CL E G H100144748201ORPHA1837212612105
HP:0012740HP:0012740Papilloma1MSH3 CL E G H4437480536ORPHA1277326600887
HP:0012740HP:0012740Papilloma1MSH3 CL E G H4437617100Familial adenomatous polyposis 4617100C4310719OMIM1277326600887
HP:0012740HP:0012740Papilloma1PIK3CA CL E G H5290201ORPHA1578975171834
HP:0012740HP:0012740Papilloma1PORCN CL E G H648402092EhrlichiosisORPHA112117652300651
HP:0012740HP:0012740Papilloma1PTEN CL E G H5728201ORPHA16589588601728
HP:0012740HP:0012740Papilloma1SDHB CL E G H6390201ORPHA127910681185470
HP:0012740HP:0012740Papilloma1SDHC CL E G H6391201ORPHA16210682602413
HP:0012740HP:0012740Papilloma1SDHD CL E G H6392201ORPHA117410683602690
HP:0012740HP:0012740Papilloma1SEC23B CL E G H10483201ORPHA112610702610512
HP:0012740HP:0012740Papilloma1SEC23B CL E G H10483616858616858616858OMIM112610702610512
HP:0012740HP:0012740Papilloma1XPA CL E G H7507910Blepharoptosis aortic anomalyORPHA15112814611153
HP:0012740HP:0012740Papilloma1XPC CL E G H7508910Blepharoptosis aortic anomalyORPHA110012816613208
HP:0012740HP:0012740Papilloma2AKT1 CL E G H207201ORPHA112391164730
HP:0012740HP:0012740Papilloma2DDB2 CL E G H1643910Blepharoptosis aortic anomalyORPHA1172718600811
HP:0012740HP:0012740Papilloma2ERCC2 CL E G H2068910Blepharoptosis aortic anomalyORPHA11083434126340
HP:0012740HP:0012740Papilloma2ERCC3 CL E G H2071910Blepharoptosis aortic anomalyORPHA1203435133510
HP:0012740HP:0012740Papilloma2ERCC4 CL E G H2072910Blepharoptosis aortic anomalyORPHA1723436133520
HP:0012740HP:0012740Papilloma2ERCC5 CL E G H2073910Blepharoptosis aortic anomalyORPHA1593437133530
HP:0012740HP:0012740Papilloma2HRAS CL E G H32653071ORPHA1345173190020
HP:0012740HP:0012740Papilloma2KLLN CL E G H100144748201ORPHA1837212612105
HP:0012740HP:0012740Papilloma2MSH3 CL E G H4437480536ORPHA1277326600887
HP:0012740HP:0012740Papilloma2MSH3 CL E G H4437617100Familial adenomatous polyposis 4617100C4310719OMIM1277326600887
HP:0012740HP:0012740Papilloma2PIK3CA CL E G H5290201ORPHA1578975171834
HP:0012740HP:0012740Papilloma2PORCN CL E G H648402092EhrlichiosisORPHA112117652300651
HP:0012740HP:0012740Papilloma2PTEN CL E G H5728201ORPHA16589588601728
HP:0012740HP:0012740Papilloma2SDHB CL E G H6390201ORPHA127910681185470
HP:0012740HP:0012740Papilloma2SDHC CL E G H6391201ORPHA16210682602413
HP:0012740HP:0012740Papilloma2SDHD CL E G H6392201ORPHA117410683602690
HP:0012740HP:0012740Papilloma2SEC23B CL E G H10483201ORPHA112610702610512
HP:0012740HP:0012740Papilloma2SEC23B CL E G H10483616858616858616858OMIM112610702610512
HP:0012740HP:0012740Papilloma2XPA CL E G H7507910Blepharoptosis aortic anomalyORPHA15112814611153
HP:0012740HP:0012740Papilloma2XPC CL E G H7508910Blepharoptosis aortic anomalyORPHA110012816613208
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012740HP:0012740Papilloma0FLT4 CL E G H2324153100Hereditary lymphedema type I153100C1704423OMIM0853767136352
HP:0012740HP:0012740Papilloma1FLT4 CL E G H2324153100Hereditary lymphedema type I153100C1704423OMIM0853767136352
HP:0012740HP:0012740Papilloma2FLT4 CL E G H2324153100Hereditary lymphedema type I153100C1704423OMIM0853767136352


Genes (41) :AKT1 BLNK CARMIL2 CD79A CD79B CXCR4 DDB2 DOCK8 ECM1 ERCC2 ERCC3 ERCC4 ERCC5 FCN3 FLT4 HRAS IGHM IGLL1 IKBKG KLLN KRT1 KRT16 KRT9 LRRC8A MSH3 NRAS PIK3CA PIK3R1 PORCN PTEN SDHB SDHC SDHD SEC23B STK4 TCF3 TMC6 TMC8 TP53 XPA XPC

Diseases (22) :201 910 153100 3071 480536 617100 2092 616858 33110 618131 193670 217390 530 613860 464 2199 249400 182000 614868 302 226400 2807
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.