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:
Abnormal emotion/affect behavior (HP:0100851)

Parent Node:
Abnormal aggressive, impulsive or violent behavior (HP:0006919)

..Starting node
..Violent behavior (HP:0008760)

Term ID:

8760

Name:

Violent behavior

Synonym:

Violent behavior; Violent behaviour

Definition:

Comments:

Reference:

HP:0008760

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aggressive behavior (HP:0000718)

Self-injurious behavior (HP:0100716)

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:0008760	HP:0008760	Violent behavior	0	PANK2 CL E G H	80025	15894	ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration	HP:0040282 - Frequent	55
HP:0008760	HP:0008760	Violent behavior	0	PIGL CL E G H	9487	8966	OMIM:280000	Zunich neuroectodermal syndrome	.	36
HP:0008760	HP:0008760	Violent behavior	0	SPTBN1 CL E G H	6711	11275	OMIM:619475	DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES; DDISBA

Genes (3) :PANK2 PIGL SPTBN1

Diseases (3) :ORPHA:216873 OMIM:280000 OMIM:619475

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