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:
Impairment in personality functioning (HP:0031466)

Parent Node:
Inappropriate behavior (HP:0000719)

..Starting node
..Inappropriate sexual behavior (HP:0008768)

Term ID:

8768

Name:

Inappropriate sexual behavior

Synonym:

Inappropriate sexual behavior; Inappropriate sexual behaviour

Definition:

Comments:

Reference:

HP:0008768

Genes and Diseases:

Child Nodes:

........

Hypersexuality (HP:0030214)

Sister Nodes:

Inappropriate crying (HP:0030215)

Inappropriate laughter (HP:0000748)

Socially inappropriate behavior (HP:0030220)

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:0008768	HP:0008768	Inappropriate sexual behavior	0	ATP7B CL E G H	540	870	ORPHA:905	Wilson disease		315
HP:0008768	HP:0008768	Inappropriate sexual behavior	0	GNAS CL E G H	2778	4392	ORPHA:562	McCune-Albright syndrome	HP:0040283 - Occasional	101
HP:0008768	HP:0008768	Inappropriate sexual behavior	0	GRN CL E G H	2896	4601	OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		126
HP:0008768	HP:0008768	Inappropriate sexual behavior	0	MAPT CL E G H	4137	6893	OMIM:600274	Frontotemporal dementia	.	140
HP:0008768	HP:0008768	Inappropriate sexual behavior	0	PSEN1 CL E G H	5663	9508	OMIM:600274	Frontotemporal dementia	.	241
HP:0008768	HP:0030214	Hypersexuality	1	ATP7B CL E G H	540	870	ORPHA:905	Wilson disease	HP:0040281 - Very frequent	315
HP:0008768	HP:0030214	Hypersexuality	1	GRN CL E G H	2896	4601	OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions	.	126

Genes (5) :ATP7B GNAS GRN MAPT PSEN1

Diseases (4) :ORPHA:905 ORPHA:562 OMIM:607485 OMIM:600274

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