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

..Starting node
..Negativism (HP:0410291)

Term ID:

410291

Name:

Negativism

Synonym:

Definition:

Opposing or not responding to instructions or external stimuli.

Comments:

Reference:

HP:0410291

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0410291	HP:0410291	Negativism	0	APOL2 CL E G H	23780	619	OMIM:181500	SCHIZOPHRENIA
HP:0410291	HP:0410291	Negativism	0	APOL4 CL E G H	80832	14867	OMIM:181500	SCHIZOPHRENIA
HP:0410291	HP:0410291	Negativism	0	CHI3L1 CL E G H	1116	1932	OMIM:181500	SCHIZOPHRENIA	1
HP:0410291	HP:0410291	Negativism	0	COMT CL E G H	1312	2228	OMIM:181500	SCHIZOPHRENIA	6
HP:0410291	HP:0410291	Negativism	0	DAOA CL E G H	267012	21191	OMIM:181500	SCHIZOPHRENIA
HP:0410291	HP:0410291	Negativism	0	DISC2 CL E G H	27184	2889	OMIM:181500	SCHIZOPHRENIA
HP:0410291	HP:0410291	Negativism	0	DRD3 CL E G H	1814	3024	OMIM:181500	SCHIZOPHRENIA	21
HP:0410291	HP:0410291	Negativism	0	HTR2A CL E G H	3356	5293	OMIM:181500	SCHIZOPHRENIA	4
HP:0410291	HP:0410291	Negativism	0	MTHFR CL E G H	4524	7436	OMIM:181500	SCHIZOPHRENIA	183
HP:0410291	HP:0410291	Negativism	0	RTN4R CL E G H	65078	18601	OMIM:181500	SCHIZOPHRENIA	2
HP:0410291	HP:0410291	Negativism	0	SYN2 CL E G H	6854	11495	OMIM:181500	SCHIZOPHRENIA	3

Genes (11) :APOL2 APOL4 CHI3L1 COMT DAOA DISC2 DRD3 HTR2A MTHFR RTN4R SYN2

Diseases (1) :OMIM:181500

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