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
..Socially inappropriate behavior (HP:0030220)

Term ID:

30220

Name:

Socially inappropriate behavior

Synonym:

Socially inappropriate behavior; Socially inappropriate behaviour

Definition:

Behavior that is not in line with social norms.

Comments:

Reference:

HP:0030220

Genes and Diseases:

Child Nodes:

Sister Nodes:

Inappropriate crying (HP:0030215)

Inappropriate laughter (HP:0000748)

Inappropriate sexual behavior (HP:0008768)

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:0030220	HP:0030220	Socially inappropriate behavior	0	VPS13A CL E G H	23230	1908	ORPHA:2388	Choreoacanthocytosis	HP:0040283 - Occasional	130

Genes (1) :VPS13A

Diseases (1) :ORPHA:2388

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