Human Phenotype Ontology

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

..Starting node
..Polyembolokoilamania (HP:0032508)

Term ID:

32508

Name:

Polyembolokoilamania

Synonym:

Definition:

Habitual insertion of foreign bodies into bodily orifices.

Comments:

Reference:

HP:0032508

Genes and Diseases:

Child Nodes:

Sister Nodes:

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:0032508	HP:0032508	Polyembolokoilamania	0	RAI1 CL E G H	10743	9834	OMIM:182290	Smith-Magenis syndrome	.	150

Genes (1) :RAI1

Diseases (1) :OMIM:182290

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