Human Phenotype Ontology

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Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Neoplasm of the skin (HP:0008069)

Parent Node:
Papilloma (HP:0012740)

..Starting node
..Verrucae (HP:0200043)

Term ID:

200043

Name:

Verrucae

Synonym:

Warts

Definition:

Warts, benign growths on the skin or mucous membranes that cause cosmetic problems as well as pain and discomfort. Warts most often occur on the hands, feet, and genital areas.

Comments:

Reference:

HP:0200043

Genes and Diseases:

Child Nodes:

........

Verruca plana (HP:0550004)

Sister Nodes:

Choroid plexus papilloma (HP:0200022)

Facial papilloma (HP:0040167)

Squamous Papilloma (HP:0031021)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0200043	HP:0200043	Verrucae	0	ATP2A2 CL E G H	488	812	ORPHA:79151	Acrokeratosis verruciformis of Hopf	HP:0040282 - Frequent	86
HP:0200043	HP:0200043	Verrucae	0	BLNK CL E G H	29760	14211	ORPHA:33110	Autosomal agammaglobulinemia	HP:0040283 - Occasional	4
HP:0200043	HP:0200043	Verrucae	0	CARMIL2 CL E G H	146206	27089	OMIM:618131	IMMUNODEFICIENCY 58; IMD58		3
HP:0200043	HP:0200043	Verrucae	0	CD4 CL E G H	920	1678	OMIM:619238	IMMUNODEFICIENCY 79; IMD79		1
HP:0200043	HP:0200043	Verrucae	0	CD79A CL E G H	973	1698	ORPHA:33110	Autosomal agammaglobulinemia	HP:0040283 - Occasional	9
HP:0200043	HP:0200043	Verrucae	0	CD79B CL E G H	974	1699	ORPHA:33110	Autosomal agammaglobulinemia	HP:0040283 - Occasional	6
HP:0200043	HP:0200043	Verrucae	0	CIB1 CL E G H	10519	16920	ORPHA:302	Epidermodysplasia verruciformis	HP:0040281 - Very frequent
HP:0200043	HP:0200043	Verrucae	0	CXCR4 CL E G H	7852	2561	ORPHA:51636	WHIM syndrome	HP:0040282 - Frequent	9
HP:0200043	HP:0200043	Verrucae	0	CXCR4 CL E G H	7852	2561	OMIM:193670	Whim syndrome		9
HP:0200043	HP:0200043	Verrucae	0	DCLRE1C CL E G H	64421	17642	ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency	HP:0040282 - Frequent	94
HP:0200043	HP:0200043	Verrucae	0	DOCK8 CL E G H	81704	19191	ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency	HP:0040281 - Very frequent	217
HP:0200043	HP:0200043	Verrucae	0	ECM1 CL E G H	1893	3153	ORPHA:530	Lipoid proteinosis	HP:0040282 - Frequent	14
HP:0200043	HP:0200043	Verrucae	0	FCN3 CL E G H	8547	3625	OMIM:613860	FICOLIN 3 DEFICIENCY		1
HP:0200043	HP:0200043	Verrucae	0	GATA2 CL E G H	2624	4171	OMIM:614038	Lymphedema, primary, with myelodysplasia		137
HP:0200043	HP:0200043	Verrucae	0	IGHM CL E G H	3507	5541	ORPHA:33110	Autosomal agammaglobulinemia	HP:0040283 - Occasional	7
HP:0200043	HP:0200043	Verrucae	0	IGLL1 CL E G H	3543	5870	ORPHA:33110	Autosomal agammaglobulinemia	HP:0040283 - Occasional	3
HP:0200043	HP:0200043	Verrucae	0	IKBKG CL E G H	8517	5961	ORPHA:464	Incontinentia pigmenti	HP:0040281 - Very frequent	52
HP:0200043	HP:0200043	Verrucae	0	IL7 CL E G H	3574	6023	ORPHA:302	Epidermodysplasia verruciformis	HP:0040281 - Very frequent
HP:0200043	HP:0200043	Verrucae	0	IL7 CL E G H	3574	6023	OMIM:618309	EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 5; EV5
HP:0200043	HP:0200043	Verrucae	0	IVNS1ABP CL E G H	10625	16951	OMIM:618969	IMMUNODEFICIENCY 70; IMD70
HP:0200043	HP:0200043	Verrucae	0	LRRC8A CL E G H	56262	19027	ORPHA:33110	Autosomal agammaglobulinemia	HP:0040283 - Occasional	3
HP:0200043	HP:0200043	Verrucae	0	PIK3R1 CL E G H	5295	8979	ORPHA:33110	Autosomal agammaglobulinemia	HP:0040283 - Occasional	43
HP:0200043	HP:0200043	Verrucae	0	SASH3 CL E G H	54440	15975	OMIM:301082			1
HP:0200043	HP:0200043	Verrucae	0	STK4 CL E G H	6789	11408	OMIM:614868	T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITHOR WITHOUT CARDIAC MALFORMATIONS	.	4
HP:0200043	HP:0200043	Verrucae	0	TCF3 CL E G H	6929	11633	ORPHA:33110	Autosomal agammaglobulinemia	HP:0040283 - Occasional	2
HP:0200043	HP:0200043	Verrucae	0	TMC6 CL E G H	11322	18021	ORPHA:302	Epidermodysplasia verruciformis	HP:0040281 - Very frequent	10
HP:0200043	HP:0200043	Verrucae	0	TMC6 CL E G H	11322	18021	OMIM:226400	Epidermodysplasia verruciformis, susceptibility to, 1	.	10
HP:0200043	HP:0200043	Verrucae	0	TMC8 CL E G H	147138	20474	ORPHA:302	Epidermodysplasia verruciformis	HP:0040281 - Very frequent	4
HP:0200043	HP:0200043	Verrucae	0	TMC8 CL E G H	147138	20474	OMIM:618231	EPIDERMODYSPLASIA VERRUCIFORMIS 2; EV2		4
HP:0200043	HP:0032301	Genital warts	1	CL E G H
HP:0200043	HP:0032215	Disseminated cutaneous warts	1	CD4 CL E G H	920	1678	OMIM:619238	IMMUNODEFICIENCY 79; IMD79		1
HP:0200043	HP:0550004	Verruca plana	1	TMC8 CL E G H	147138	20474	OMIM:618231	EPIDERMODYSPLASIA VERRUCIFORMIS 2; EV2		4

Genes (25) :ATP2A2 BLNK CARMIL2 CD4 CD79A CD79B CIB1 CXCR4 DCLRE1C DOCK8 ECM1 FCN3 GATA2 IGHM IGLL1 IKBKG IL7 IVNS1ABP LRRC8A PIK3R1 SASH3 STK4 TCF3 TMC6 TMC8

Diseases (19) :ORPHA:79151 ORPHA:33110 OMIM:618131 OMIM:619238 ORPHA:302 ORPHA:51636 OMIM:193670 ORPHA:275 ORPHA:217390 ORPHA:530 OMIM:613860 OMIM:614038 ORPHA:464 OMIM:618309 OMIM:618969 OMIM:301082 OMIM:614868 OMIM:226400 OMIM:618231

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.

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