Tunnus
Hallucinations
Perceptions in a conscious and awake state that, in the absence of external stimuli, have qualities of real perception. These perceptions are vivid, substantial, and located in external objective space.
Kokkuvõte
- Teised nimetused
- Hallucination, Sensory hallucination
- Kehasüsteem
- Abnormality of the nervous system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
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Telli oma Genome Test117 geeni on seotud tunnusega Hallucinations
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Hallucinations. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| GCSHglycine cleavage system protein H | Alati | Esineb 1 haiguses |
| HTRA1HtrA serine peptidase 1 | Alati | Esineb 1 haiguses |
| LRRC7leucine rich repeat containing 7 | Alati | Esineb 1 haiguses |
| RAB3ARAB3A, member RAS oncogene family | Alati | Esineb 1 haiguses |
| TRRAPtransformation/transcription domain associated protein | Alati | Esineb 1 haiguses |
| APPamyloid beta precursor protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| CLTRNcollectrin, amino acid transport regulator | Väga sageli (80–99%) | Esineb 1 haiguses |
| CTSHcathepsin H | Väga sageli (80–99%) | Esineb 1 haiguses |
| HCRThypocretin neuropeptide precursor | Väga sageli (80–99%) | Esineb 2 haiguses |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| MOGmyelin oligodendrocyte glycoprotein | Väga sageli (80–99%) | Esineb 1 haiguses |
| P2RY11purinergic receptor P2Y11 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PSEN1presenilin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PSEN2presenilin 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC6A19solute carrier family 6 member 19 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SORL1sortilin related receptor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TNFSF4TNF superfamily member 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TOMM40translocase of outer mitochondrial membrane 40 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TREM2triggering receptor expressed on myeloid cells 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZNF365zinc finger protein 365 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ARSAarylsulfatase A | Sageli (30–79%) | Esineb 4 haiguses |
| ATP13A2ATPase cation transporting 13A2 | Sageli (30–79%) | Esineb 3 haiguses |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Sageli (30–79%) | Esineb 2 haiguses |
| EPG5ectopic P-granules 5 autophagy tethering factor | Sageli (30–79%) | Esineb 1 haiguses |
| FUSFUS RNA binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| HTRA2HtrA serine peptidase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| HTThuntingtin | Sageli (30–79%) | Esineb 1 haiguses |
| LRRK2leucine rich repeat kinase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PARK7Parkinsonism associated deglycase | Sageli (30–79%) | Esineb 1 haiguses |
| PINK1PTEN induced kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PODXLpodocalyxin like | Sageli (30–79%) | Esineb 1 haiguses |
| PRKNparkin RBR E3 ubiquitin protein ligase | Sageli (30–79%) | Esineb 1 haiguses |
| PRNPprion protein (Kanno blood group) | Sageli (30–79%) | Esineb 3 haiguses |
| PSAPprosaposin | Sageli (30–79%) | Esineb 3 haiguses |
| RAB32RAB32, member RAS oncogene family | Sageli (30–79%) | Esineb 1 haiguses |
| SLC25A13solute carrier family 25 member 13 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC2A3solute carrier family 2 member 3 | Sageli (30–79%) | Esineb 1 haiguses |
| SNCAsynuclein alpha | Sageli (30–79%) | Esineb 3 haiguses |
Näita veel 77 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| SQSTM1sequestosome 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SYNJ1synaptojanin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TARDBPTAR DNA binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| TBK1TANK binding kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| UCHL1ubiquitin C-terminal hydrolase L1 | Sageli (30–79%) | Esineb 1 haiguses |
| VCPvalosin containing protein | Sageli (30–79%) | Esineb 1 haiguses |
| VPS13Cvacuolar protein sorting 13 homolog C | Sageli (30–79%) | Esineb 2 haiguses |
| ADH1Calcohol dehydrogenase 1C (class I), gamma polypeptide | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALADaminolevulinate dehydratase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATMATM serine/threonine kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP7BATPase copper transporting beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATXN2ataxin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATXN3ataxin 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATXN8OSATXN8 opposite strand lncRNA | Mõnikord (5–29%) | Esineb 1 haiguses |
| BMPR1Abone morphogenetic protein receptor type 1A | Mõnikord (5–29%) | Esineb 1 haiguses |
| BPTFbromodomain PHD finger transcription factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRCA2BRCA2 DNA repair associated | Mõnikord (5–29%) | Esineb 1 haiguses |
| CHEK2checkpoint kinase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CISD2CDGSH iron sulfur domain 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| DCAF17DDB1 and CUL4 associated factor 17 | Mõnikord (5–29%) | Esineb 2 haiguses |
| EPCAMepithelial cell adhesion molecule | Mõnikord (5–29%) | Esineb 1 haiguses |
| GBA1glucosylceramidase beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HMBShydroxymethylbilane synthase | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRASKRas proto-oncogene, GTPase | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAN2B1mannosidase alpha class 2B member 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MAPTmicrotubule associated protein tau | Mõnikord (5–29%) | Esineb 1 haiguses |
| MED12mediator complex subunit 12 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MLH1mutL homolog 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MSH2mutS homolog 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MSH6mutS homolog 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TTmitochondrially encoded tRNA-Thr (ACN) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MUTYHmutY DNA glycosylase | Mõnikord (5–29%) | Esineb 1 haiguses |
| NDPnorrin cystine knot growth factor NDP | Mõnikord (5–29%) | Esineb 2 haiguses |
| NPATnuclear protein, coactivator of histone transcription | Mõnikord (5–29%) | Esineb 1 haiguses |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| PMS1PMS1 homolog 1, mismatch repair system component | Mõnikord (5–29%) | Esineb 1 haiguses |
| PMS2PMS1 homolog 2, mismatch repair system component | Mõnikord (5–29%) | Esineb 1 haiguses |
| POLD1DNA polymerase delta 1, catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| POLEDNA polymerase epsilon, catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RPS20ribosomal protein S20 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SEMA4Asemaphorin 4A | Mõnikord (5–29%) | Esineb 1 haiguses |
| SNCAIPsynuclein alpha interacting protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPARTspartin | Mõnikord (5–29%) | Esineb 1 haiguses |
| TBPTATA-box binding protein | Mõnikord (5–29%) | Esineb 2 haiguses |
| TGFBR2transforming growth factor beta receptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TTRtransthyretin | Mõnikord (5–29%) | Esineb 1 haiguses |
| UPF3BUPF3B regulator of nonsense mediated mRNA decay | Mõnikord (5–29%) | Esineb 1 haiguses |
| WFS1wolframin ER transmembrane glycoprotein | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZDHHC9zDHHC palmitoyltransferase 9 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DNM1Ldynamin 1L | Harva (1–4%) | Esineb 1 haiguses |
| OPA1OPA1 mitochondrial dynamin like GTPase | Harva (1–4%) | Esineb 1 haiguses |
| PPIBpeptidylprolyl isomerase B | Harva (1–4%) | Esineb 1 haiguses |
| PPOXprotoporphyrinogen oxidase | Harva (1–4%) | Esineb 1 haiguses |
| ALDH5A1aldehyde dehydrogenase 5 family member A1 | Pole registreeritud | Esineb 1 haiguses |
| APOL2apolipoprotein L2 | Pole registreeritud | Esineb 1 haiguses |
| BCKDHAbranched chain keto acid dehydrogenase E1 subunit alpha | Pole registreeritud | Esineb 1 haiguses |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Pole registreeritud | Esineb 1 haiguses |
| C9orf72C9orf72-SMCR8 complex subunit | Pole registreeritud | Esineb 1 haiguses |
| CHI3L1chitinase 3 like 1 | Pole registreeritud | Esineb 1 haiguses |
| CPOXcoproporphyrinogen oxidase | Pole registreeritud | Esineb 1 haiguses |
| DAOAD-amino acid oxidase activator | Pole registreeritud | Esineb 1 haiguses |
| DISC2disrupted in schizophrenia 2 | Pole registreeritud | Esineb 1 haiguses |
| DRD3dopamine receptor D3 | Pole registreeritud | Esineb 1 haiguses |
| ECM1extracellular matrix protein 1 | Pole registreeritud | Esineb 1 haiguses |
| GRNgranulin precursor | Pole registreeritud | Esineb 1 haiguses |
| HTR2A5-hydroxytryptamine receptor 2A | Pole registreeritud | Esineb 1 haiguses |
| JPH3junctophilin 3 | Pole registreeritud | Esineb 1 haiguses |
| MTHFRmethylenetetrahydrofolate reductase | Pole registreeritud | Esineb 1 haiguses |
| PPT1palmitoyl-protein thioesterase 1 | Pole registreeritud | Esineb 1 haiguses |
| PRDM8PR/SET domain 8 | Pole registreeritud | Esineb 1 haiguses |
| RTN4Rreticulon 4 receptor | Pole registreeritud | Esineb 1 haiguses |
| SYN2synapsin II | Pole registreeritud | Esineb 1 haiguses |
| TTC19tetratricopeptide repeat domain 19 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Kitsamad tunnused
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.16-c6eea6bf.
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Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast