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

Grandparent Node:
Inappropriate behavior (HP:0000719)

Parent Node:
Inappropriate sexual behavior (HP:0008768)

..Starting node
..Hypersexuality (HP:0030214)

Term ID:

30214

Name:

Hypersexuality

Synonym:

Sex addiction

Definition:

Pathological persistent sexual disinhibiting behavior, directed at oneself or to others.

Comments:

Reference:

HP:0030214

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:0030214	HP:0030214	Hypersexuality	0	ATP7B CL E G H	540	870	ORPHA:905	Wilson disease	HP:0040281 - Very frequent	315
HP:0030214	HP:0030214	Hypersexuality	0	GRN CL E G H	2896	4601	OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions	.	126

Genes (2) :ATP7B GRN

Diseases (2) :ORPHA:905 OMIM:607485

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