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

 

Gene

ENSG00000133048 - chitinase 3 like 1

Gene

ENSG00000108679 - galectin 3 binding protein

Gene

ENSG00000118849 - retinoic acid receptor responder 1

Gene

ENSG00000125144 - metallothionein 1G

Gene

ENSG00000079385 - CEA cell adhesion molecule 1

Gene

ENSG00000197594 - ectonucleotide pyrophosphatase/phosphodiesterase 1

Gene

ENSG00000064651 - solute carrier family 12 member 2

Gene

ENSG00000291237 - superoxide dismutase 2

Gene

ENSG00000205426 - keratin 81

Gene

ENSG00000197746 - prosaposin

  • Gene

    ENSG00000133048 - chitinase 3 like 1


  • Gene

    ENSG00000108679 - galectin 3 binding protein


  • Gene

    ENSG00000118849 - retinoic acid receptor responder 1


  • Gene

    ENSG00000125144 - metallothionein 1G


  • Gene

    ENSG00000079385 - CEA cell adhesion molecule 1


  • Gene

    ENSG00000197594 - ectonucleotide pyrophosphatase/phosphodiesterase 1


  • Gene

    ENSG00000064651 - solute carrier family 12 member 2


  • Gene

    ENSG00000291237 - superoxide dismutase 2


  • Gene

    ENSG00000205426 - keratin 81


  • Gene

    ENSG00000197746 - prosaposin

  • DISPLAY PER PAGE
    This repository is under review for potential modification in compliance with Administration directives.