AtlasTræk
Disturbances of consciousness
Klinisk navn: Reduced consciousness
Abnormally diminished level of attention, responsiveness, or wakefulness.
Resumé
- Også kaldet
- Lowered consciousness, Reduced consciousness/confusion
- Kropssystem
- Abnormality of the nervous system
AtlasDenne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/reduced-consciousness.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Disturbances of consciousness, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test25 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Hereditary Optic NeuropathyReads 5 of these genesATP1A3MT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Systemic Lupus ErythematosusReads 2 of these genesUNC93B1SAT1About this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 2 of these genesCASRGNA11About this report →
- Cerebral Amyloid AngiopathyReads 1 of these genesCST3About this report →
Show 21 more reports
- Hereditary Fructose Intolerance & Gluconeogenesis DefectsReads 1 of these genesFBP1About this report →
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 1 of these genesSMARCB1About this report →
- Thyroid CancerReads 3 of these genesMEN1CASRGNA11About this report →
- NeurofibromatosisReads 1 of these genesSMARCB1About this report →
- Leigh SyndromeReads 4 of these genesMT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Autoimmune DiseaseReads 2 of these genesUNC93B1SAT1About this report →
- Classic Organic AciduriasReads 1 of these genesACAT1About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesMEN1About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 1 of these genesIL12BAbout this report →
- Inherited Neurodegenerative DisordersReads 6 of these genesATP1A3TBK1MT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Coffin-Siris SyndromeReads 1 of these genesSMARCB1About this report →
- Hereditary AmyloidosisReads 1 of these genesCST3About this report →
- Frontotemporal DementiaReads 1 of these genesTBK1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesMT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesTBK1About this report →
- Diabetes MellitusReads 1 of these genesMT-TL1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesATP1A3About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesATP1A3About this report →
- Epilepsy (Full Panel)Reads 1 of these genesATP1A3About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesMYD88About this report →
- Intellectual DisabilityReads 1 of these genesSMARCB1About this report →
Læs de gener, der er knyttet til Disturbances of consciousness, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test37 gener knyttet til Disturbances of consciousness
Ændringer i disse gener forårsager sjældne tilstande, hvor Disturbances of consciousness ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| ABCB1ATP binding cassette subfamily B member 1 | Altid | I 1 tilstand |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Altid | I 1 tilstand |
| TBK1TANK binding kinase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| TICAM1TIR domain containing adaptor molecule 1 | Meget ofte (80–99 %) | I 1 tilstand |
| TLR3toll like receptor 3 | Meget ofte (80–99 %) | I 1 tilstand |
| TRAF3TNF receptor associated factor 3 | Meget ofte (80–99 %) | I 1 tilstand |
| UNC93B1unc-93B1 regulator of TLR signaling | Meget ofte (80–99 %) | I 1 tilstand |
| ACAT1acetyl-CoA acetyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| CST3cystatin C | Ofte (30–79 %) | I 1 tilstand |
| MEN1menin 1 | Ofte (30–79 %) | I 1 tilstand |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Ofte (30–79 %) | I 1 tilstand |
| YY1YY1 transcription factor | Ofte (30–79 %) | I 1 tilstand |
| CASRcalcium sensing receptor | Nogle gange (5–29 %) | I 1 tilstand |
| FBP1fructose-bisphosphatase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GNA11G protein subunit alpha 11 | Nogle gange (5–29 %) | I 1 tilstand |
| HLA-Bmajor histocompatibility complex, class I, B | Nogle gange (5–29 %) | I 1 tilstand |
| IL12Binterleukin 12B | Nogle gange (5–29 %) | I 1 tilstand |
| IRAK1interleukin 1 receptor associated kinase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MLXMAX dimerization protein MLX | Nogle gange (5–29 %) | I 1 tilstand |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Nogle gange (5–29 %) | I 1 tilstand |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Nogle gange (5–29 %) | I 1 tilstand |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Nogle gange (5–29 %) | I 1 tilstand |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Nogle gange (5–29 %) | I 1 tilstand |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Nogle gange (5–29 %) | I 1 tilstand |
| MYD88MYD88 innate immune signal transduction adaptor | Nogle gange (5–29 %) | I 1 tilstand |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SPP1secreted phosphoprotein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| STAT4signal transducer and activator of transcription 4 | Nogle gange (5–29 %) | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Snævrere træk
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
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