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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 41 - 50 of 57 in total
Gene ID Gene Symbol Description Source
7804 LRP8 LDL receptor related protein 8
7976 FZD3 frizzled class receptor 3
8516 ITGA8 integrin subunit alpha 8
8911 CACNA1I calcium voltage-gated channel subunit alpha1 I
10752 CHL1 cell adhesion molecule L1 like
23191 CYFIP1 cytoplasmic FMR1 interacting protein 1
23385 NCSTN nicastrin
23774 BRD1 bromodomain containing 1
26047 CNTNAP2 contactin associated protein 2
27086 FOXP1 forkhead box P1
Displaying entries 21 - 30 of 32 in total
Gene ID Gene Symbol Description Source
58234 Shank3 SH3 and multiple ankyrin repeat domains 3
59287 Ncstn nicastrin
74342 Lrrtm1 leucine rich repeat transmembrane neuronal 1
94109 Csmd1 CUB and Sushi multiple domains 1
108071 Grm5 glutamate receptor, metabotropic 5
111174 Taar1 trace amine-associated receptor 1
216856 Nlgn2 neuroligin 2
225207 Zfp521 zinc finger protein 521
232333 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1
233904 Setd1a SET domain containing 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:0000746 Delusion
HP:0100753 Schizophrenia
HP:0007086 Social and occupational deterioration
HP:0000738 Hallucinations
HP:0002353 EEG abnormality
HP:0000006 Autosomal dominant inheritance
Displaying all 3 entries
Gene ID Gene Symbol Description
1312 COMT catechol-O-methyltransferase
65078 RTN4R reticulon 4 receptor
1116 CHI3L1 chitinase 3 like 1
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: August 4, 2025