Schizophrenia (Phenotype)

Id:HP:0100753

Description:A mental disorder characterized by a disintegration of thought processes and emotional responsiveness. It most commonly manifests as auditory hallucinations, paranoid or bizarre delusions, or disorganized speech and thinking. It is accompanied by significant social or occupational dysfunction. The onset of symptoms typically occurs in young adulthood, with a global lifetime prevalence of about 1%. This term is not a helpful parent term to describe abnormal experiences.

Results found

Linked to

	Label	Description
	CHRNA7 Gene (Entity type)	ENSG00000282088 - cholinergic receptor nicotinic alpha 7 subunit [Source:HGNC Symbol;Acc:HGNC:1960]
	SU001142 Subject (Entity type)	A subject from Metabolomics produced as part of the PR000734 project
	SHANK3 Gene (Entity type)	ENSG00000251322 - SH3 and multiple ankyrin repeat domains 3
	MT1G Gene (Entity type)	ENSG00000125144 - metallothionein 1G
	NKX2-1 Gene (Entity type)	ENSG00000136352 - NK2 homeobox 1
	REV3L Gene (Entity type)	ENSG00000009413 - REV3 like, DNA directed polymerase zeta catalytic subunit
	APOL4 Gene (Entity type)	ENSG00000100336 - apolipoprotein L4
	BTN3A2 Gene (Entity type)	ENSG00000186470 - butyrophilin subfamily 3 member A2
	MYO7A Gene (Entity type)	ENSG00000137474 - myosin VIIA
	PDZD7 Gene (Entity type)	ENSG00000186862 - PDZ domain containing 7

CHRNA7

Gene (Entity type)

ENSG00000282088 - cholinergic receptor nicotinic alpha 7 subunit [Source:HGNC Symbol;Acc:HGNC:1960]

SU001142

Subject (Entity type)

A subject from Metabolomics produced as part of the PR000734 project

SHANK3

Gene (Entity type)

ENSG00000251322 - SH3 and multiple ankyrin repeat domains 3

MT1G

Gene (Entity type)

ENSG00000125144 - metallothionein 1G

NKX2-1

Gene (Entity type)

ENSG00000136352 - NK2 homeobox 1

REV3L

Gene (Entity type)

ENSG00000009413 - REV3 like, DNA directed polymerase zeta catalytic subunit

APOL4

Gene (Entity type)

ENSG00000100336 - apolipoprotein L4

BTN3A2

Gene (Entity type)

ENSG00000186470 - butyrophilin subfamily 3 member A2

MYO7A

Gene (Entity type)

ENSG00000137474 - myosin VIIA

PDZD7

Gene (Entity type)

ENSG00000186862 - PDZ domain containing 7

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Consortium

Community

Resources

CFDE Workbench

The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

@CFDE Workbench 2026

This repository is under review for potential modification in compliance with Administration directives.