Hvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørKom i gangfra 449 $
Egenskap
Psychosis
A condition characterized by changes in personality and thought patterns, often accompanied by hallucinations and delusional beliefs, is known as psychosis.
Sammendrag
- Kroppssystem
- Abnormality of the nervous system
PsychosisHP:0000709
Hvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørKom i gangfra 449 $
Read the genes linked to Psychosis, and the rest of your genome, with one test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test147 gener knyttet til Psychosis
Endringer i disse genene forårsaker sjeldne tilstander der Psychosis forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| LRRC7leucine rich repeat containing 7 | Alltid | I 1 tilstand |
| MMADHCmetabolism of cobalamin associated D | Alltid | I 1 tilstand |
| NOTCH3notch receptor 3 | Alltid | I 1 tilstand |
| RFC4replication factor C subunit 4 | Alltid | I 1 tilstand |
| TBC1D7TBC1 domain family member 7 | Alltid | I 1 tilstand |
| TRRAPtransformation/transcription domain associated protein | Alltid | I 1 tilstand |
| UNC13Aunc-13 homolog A | Alltid | I 1 tilstand |
| WFS1wolframin ER transmembrane glycoprotein | Svært ofte (80–99 %) | I 1 tilstand |
| CMPK2cytidine/uridine monophosphate kinase 2 | Ofte (30–79 %) | I 1 tilstand |
| DNMT1DNA methyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| H4C3H4 clustered histone 3 | Ofte (30–79 %) | I 1 tilstand |
| JAM2junctional adhesion molecule 2 | Ofte (30–79 %) | I 2 tilstander |
| MAGEL2MAGE family member L2 | Ofte (30–79 %) | I 5 tilstander |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Ofte (30–79 %) | I 1 tilstand |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Ofte (30–79 %) | I 1 tilstand |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Ofte (30–79 %) | I 1 tilstand |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Ofte (30–79 %) | I 1 tilstand |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Ofte (30–79 %) | I 1 tilstand |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Ofte (30–79 %) | I 1 tilstand |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Ofte (30–79 %) | I 1 tilstand |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Ofte (30–79 %) | I 1 tilstand |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Ofte (30–79 %) | I 1 tilstand |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Ofte (30–79 %) | I 1 tilstand |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Ofte (30–79 %) | I 1 tilstand |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Ofte (30–79 %) | I 1 tilstand |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Ofte (30–79 %) | I 1 tilstand |
| MYORGmyogenesis regulating glycosidase | Ofte (30–79 %) | I 3 tilstander |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | Ofte (30–79 %) | I 3 tilstander |
| NDNnecdin, MAGE family member | Ofte (30–79 %) | I 3 tilstander |
| NDPnorrin cystine knot growth factor NDP | Ofte (30–79 %) | I 2 tilstander |
| OCA2OCA2 melanosomal transmembrane protein | Ofte (30–79 %) | I 3 tilstander |
| PDGFBplatelet derived growth factor subunit B | Ofte (30–79 %) | I 3 tilstander |
| PDGFRBplatelet derived growth factor receptor beta | Ofte (30–79 %) | I 2 tilstander |
| RRP12ribosomal RNA processing 12 homolog | Ofte (30–79 %) | I 1 tilstand |
| SLC20A2solute carrier family 20 member 2 | Ofte (30–79 %) | I 2 tilstander |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Ofte (30–79 %) | I 3 tilstander |
| TPM2tropomyosin 2 | Ofte (30–79 %) | I 1 tilstand |
| WARS2tryptophanyl tRNA synthetase 2, mitochondrial | Ofte (30–79 %) | I 1 tilstand |
| XPR1xenotropic and polytropic retrovirus receptor 1 | Ofte (30–79 %) | I 2 tilstander |
Vis 107 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| AARS2alanyl-tRNA synthetase 2, mitochondrial | Noen ganger (5–29 %) | I 1 tilstand |
| ACADSacyl-CoA dehydrogenase short chain | Noen ganger (5–29 %) | I 1 tilstand |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Noen ganger (5–29 %) | I 1 tilstand |
| ASLargininosuccinate lyase | Noen ganger (5–29 %) | I 1 tilstand |
| ATP7BATPase copper transporting beta | Noen ganger (5–29 %) | I 1 tilstand |
| ATXN7ataxin 7 | Noen ganger (5–29 %) | I 1 tilstand |
| BRD4bromodomain containing 4 | Noen ganger (5–29 %) | I 1 tilstand |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Noen ganger (5–29 %) | I 2 tilstander |
| CBScystathionine beta-synthase | Noen ganger (5–29 %) | I 1 tilstand |
| CHD2chromodomain helicase DNA binding protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| CHD8chromodomain helicase DNA binding protein 8 | Noen ganger (5–29 %) | I 1 tilstand |
| CHMP2Bcharged multivesicular body protein 2B | Noen ganger (5–29 %) | I 1 tilstand |
| CLTRNcollectrin, amino acid transport regulator | Noen ganger (5–29 %) | I 1 tilstand |
| CPOXcoproporphyrinogen oxidase | Noen ganger (5–29 %) | I 1 tilstand |
| CUX2cut like homeobox 2 | Noen ganger (5–29 %) | I 1 tilstand |
| DCAF17DDB1 and CUL4 associated factor 17 | Noen ganger (5–29 %) | I 2 tilstander |
| DNM1dynamin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| EHMT1euchromatic histone lysine methyltransferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GABRB3gamma-aminobutyric acid type A receptor subunit beta3 | Noen ganger (5–29 %) | I 1 tilstand |
| GCLCglutamate-cysteine ligase catalytic subunit | Noen ganger (5–29 %) | I 1 tilstand |
| GRNgranulin precursor | Noen ganger (5–29 %) | I 1 tilstand |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| IRAK1interleukin 1 receptor associated kinase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| JARID2jumonji and AT-rich interaction domain containing 2 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNN2potassium calcium-activated channel subfamily N member 2 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNT1potassium sodium-activated channel subfamily T member 1 | Noen ganger (5–29 %) | I 1 tilstand |
| KDM6Blysine demethylase 6B | Noen ganger (5–29 %) | I 1 tilstand |
| MAPK10mitogen-activated protein kinase 10 | Noen ganger (5–29 %) | I 1 tilstand |
| MAPTmicrotubule associated protein tau | Noen ganger (5–29 %) | I 1 tilstand |
| MECP2methyl-CpG binding protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| MED12mediator complex subunit 12 | Noen ganger (5–29 %) | I 2 tilstander |
| MKRN3makorin ring finger protein 3 | Noen ganger (5–29 %) | I 1 tilstand |
| MTHFRmethylenetetrahydrofolate reductase | Noen ganger (5–29 %) | I 1 tilstand |
| NIT1nitrilase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| NPAP1nuclear pore associated protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PAK3p21 (RAC1) activated kinase 3 | Noen ganger (5–29 %) | I 1 tilstand |
| PIDD1p53-induced death domain protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PRORPprotein only RNase P catalytic subunit | Noen ganger (5–29 %) | I 1 tilstand |
| PSEN1presenilin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PUS3pseudouridine synthase 3 | Noen ganger (5–29 %) | I 1 tilstand |
| PWAR1Prader Willi/Angelman region RNA 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Noen ganger (5–29 %) | I 1 tilstand |
| RPS6KA3ribosomal protein S6 kinase A3 | Noen ganger (5–29 %) | I 1 tilstand |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SIM1SIM bHLH transcription factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC25A13solute carrier family 25 member 13 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC6A19solute carrier family 6 member 19 | Noen ganger (5–29 %) | I 2 tilstander |
| SMAD4SMAD family member 4 | Noen ganger (5–29 %) | I 1 tilstand |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Noen ganger (5–29 %) | I 1 tilstand |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Noen ganger (5–29 %) | I 1 tilstand |
| SOBPsine oculis binding protein homolog | Noen ganger (5–29 %) | I 1 tilstand |
| SPARTspartin | Noen ganger (5–29 %) | I 1 tilstand |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Noen ganger (5–29 %) | I 1 tilstand |
| SPP1secreted phosphoprotein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SQSTM1sequestosome 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SRCAPSnf2 related CREBBP activator protein | Noen ganger (5–29 %) | I 1 tilstand |
| STAT4signal transducer and activator of transcription 4 | Noen ganger (5–29 %) | I 1 tilstand |
| TMEM106Btransmembrane protein 106B | Noen ganger (5–29 %) | I 2 tilstander |
| TREM2triggering receptor expressed on myeloid cells 2 | Noen ganger (5–29 %) | I 1 tilstand |
| TREX1three prime repair exonuclease 1 | Noen ganger (5–29 %) | I 2 tilstander |
| UPF3BUPF3B regulator of nonsense mediated mRNA decay | Noen ganger (5–29 %) | I 1 tilstand |
| VCPvalosin containing protein | Noen ganger (5–29 %) | I 1 tilstand |
| ZDHHC9zDHHC palmitoyltransferase 9 | Noen ganger (5–29 %) | I 1 tilstand |
| ZMYM2zinc finger MYM-type containing 2 | Noen ganger (5–29 %) | I 1 tilstand |
| ATRXATRX chromatin remodeler | Sjelden (1–4%) | I 1 tilstand |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Sjelden (1–4%) | I 1 tilstand |
| CDH23cadherin related 23 | Sjelden (1–4%) | I 1 tilstand |
| CTSHcathepsin H | Sjelden (1–4%) | I 1 tilstand |
| EIF3Feukaryotic translation initiation factor 3 subunit F | Sjelden (1–4%) | I 1 tilstand |
| FTLferritin light chain | Sjelden (1–4%) | I 1 tilstand |
| HCRThypocretin neuropeptide precursor | Sjelden (1–4%) | I 1 tilstand |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Sjelden (1–4%) | I 1 tilstand |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sjelden (1–4%) | I 1 tilstand |
| MMACHCmetabolism of cobalamin associated C | Sjelden (1–4%) | I 1 tilstand |
| MOGmyelin oligodendrocyte glycoprotein | Sjelden (1–4%) | I 1 tilstand |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Sjelden (1–4%) | I 1 tilstand |
| P2RY11purinergic receptor P2Y11 | Sjelden (1–4%) | I 1 tilstand |
| PANK2pantothenate kinase 2 | Sjelden (1–4%) | I 1 tilstand |
| PCDH19protocadherin 19 | Sjelden (1–4%) | I 2 tilstander |
| TNFSF4TNF superfamily member 4 | Sjelden (1–4%) | I 1 tilstand |
| TP53tumor protein p53 | Sjelden (1–4%) | I 1 tilstand |
| USP48ubiquitin specific peptidase 48 | Sjelden (1–4%) | I 1 tilstand |
| USP8ubiquitin specific peptidase 8 | Sjelden (1–4%) | I 1 tilstand |
| ZNF365zinc finger protein 365 | Sjelden (1–4%) | I 1 tilstand |
| ABCD1ATP binding cassette subfamily D member 1 | Ikke registrert | I 1 tilstand |
| ALDH5A1aldehyde dehydrogenase 5 family member A1 | Ikke registrert | I 1 tilstand |
| CLN3CLN3 lysosomal/endosomal transmembrane protein, battenin | Ikke registrert | I 1 tilstand |
| DNASE1deoxyribonuclease 1 | Ikke registrert | I 1 tilstand |
| EPM2AEPM2A glucan phosphatase, laforin | Ikke registrert | I 1 tilstand |
| FCGR2AFc gamma receptor IIa | Ikke registrert | I 1 tilstand |
| FCGR2BFc gamma receptor IIb | Ikke registrert | I 1 tilstand |
| GNASGNAS complex locus | Ikke registrert | I 1 tilstand |
| ITM2Bintegral membrane protein 2B | Ikke registrert | I 1 tilstand |
| NPC1NPC intracellular cholesterol transporter 1 | Ikke registrert | I 1 tilstand |
| NPC2NPC intracellular cholesterol transporter 2 | Ikke registrert | I 1 tilstand |
| PAHphenylalanine hydroxylase | Ikke registrert | I 1 tilstand |
| PDE11Aphosphodiesterase 11A | Ikke registrert | I 1 tilstand |
| PPOXprotoporphyrinogen oxidase | Ikke registrert | I 1 tilstand |
| PRDM8PR/SET domain 8 | Ikke registrert | I 1 tilstand |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Ikke registrert | I 1 tilstand |
| PRNPprion protein (Kanno blood group) | Ikke registrert | I 1 tilstand |
| SLC12A6solute carrier family 12 member 6 | Ikke registrert | I 1 tilstand |
| TTC19tetratricopeptide repeat domain 19 | Ikke registrert | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Ikke registrert | I 1 tilstand |
| VPS13Avacuolar protein sorting 13 homolog A | Ikke registrert | I 1 tilstand |
| ZFYVE26zinc finger FYVE-type containing 26 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.16-c6eea6bf.
Hvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørKom i gangfra 449 $
Én test. En livstid med svar.
Fra 449 $Gratis frakt · Resultater på 6–8 uker