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Standards Ontologies Notations
Guidelines
MIRAGE
schizophrenia

Summary
Synonym
  • schizophrenia-1
Definition
A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.
Super Class
psychotic disorder
Disease Ontology
DOID:5419
MeSH
UMLS
NCI Thesaurus
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 21 - 30 of 57 in total
Gene ID Gene Symbol Description Source
3305 HSPA1L heat shock protein family A (Hsp70) member 1 like
3356 HTR2A 5-hydroxytryptamine receptor 2A
3358 HTR2C 5-hydroxytryptamine receptor 2C
3586 IL10 interleukin 10
3613 IMPA2 inositol monophosphatase 2
3782 KCNN3 potassium calcium-activated channel subfamily N member 3
3897 L1CAM L1 cell adhesion molecule
4855 NOTCH4 notch receptor 4
4914 NTRK1 neurotrophic receptor tyrosine kinase 1
4923 NTSR1 neurotensin receptor 1
Displaying entries 11 - 20 of 32 in total
Gene ID Gene Symbol Description Source
18596 Pdgfrb platelet derived growth factor receptor, beta polypeptide
19013 Ppara peroxisome proliferator activated receptor alpha
19699 Reln reelin
20614 Snap25 synaptosomal-associated protein 25
21413 Tcf4 transcription factor 4
22631 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide
23821 Bace1 beta-site APP cleaving enzyme 1
27364 Srr serine racemase
53374 Chst3 carbohydrate sulfotransferase 3
54140 Avpr1a arginine vasopressin receptor 1A
Displaying all 3 entries
Gene ID Gene Symbol Description Source
24598 Nos1 nitric oxide synthase 1
25248 Cnr1 cannabinoid receptor 1
29595 Htr2a 5-hydroxytryptamine receptor 2A
Displaying 1 entry
Gene ID Gene Symbol Description Source
47220 Fur1 Furin 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
403310 cacna1da calcium channel, voltage-dependent, L type, alpha 1D subunit, a
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P30430 Furin-like protease 1, isoform 1-CRR
The Human Phenotype Ontology
Displaying all 6 entries
HPO ID HPO Term
HP:0002353 EEG abnormality
HP:0000738 Hallucinations
HP:0100753 Schizophrenia
HP:0000006 Autosomal dominant inheritance
HP:0007086 Social and occupational deterioration
HP:0000746 Delusion
Displaying all 3 entries
Gene ID Gene Symbol Description
1116 CHI3L1 chitinase 3 like 1
1312 COMT catechol-O-methyltransferase
65078 RTN4R reticulon 4 receptor
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025