Human Phenotype Ontology

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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

..Starting node
..Disseminated cutaneous warts (HP:0032215)

Term ID:

32215

Name:

Disseminated cutaneous warts

Synonym:

Definition:

Multiple skin warts located in multiple parts of the body, e.g., neck, trunks, and extremities.

Comments:

Reference:

HP:0032215

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0032215	HP:0032215	Disseminated cutaneous warts	0	CD4 CL E G H	920	1678	OMIM:619238	IMMUNODEFICIENCY 79; IMD79	1

Genes (1) :CD4

Diseases (1) :OMIM:619238

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