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Egenskap
Liver failure
Klinisk navn: Hepatic failure
Sammendrag
- Også kalt
- Hepatic insufficiency
- Kroppssystem
- Abnormality of the digestive system
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Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/hepatic-failure.json"
page <- fromJSON(url)
page$trait$nameLiver failureHP:0001399
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Les genene knyttet til Liver failure, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test70 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.
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 13 of these genesPEX19PEX1PEX10PEX11BPEX12PEX13About this report →
- Dyskeratosis CongenitaReads 13 of these genesPOT1ACDCTC1DKC1NHP2NOP10About this report →
- Hereditary Hemorrhagic TelangiectasiaReads 4 of these genesACVRL1ENGGDF2SMAD4About this report →
- Other Inherited LeukodystrophiesReads 13 of these genesPEX19PEX1PEX10PEX11BPEX12PEX13About this report →
Show 66 more reports
- Leigh SyndromeReads 12 of these genesGFM1SERAC1DLDMT-ATP6MT-ND1MT-ND3About this report →
- Familial Pulmonary FibrosisReads 4 of these genesPOT1PARNRTEL1TERTAbout this report →
- Urea Cycle DisorderReads 4 of these genesOTCSLC7A7ASLSLC25A15About this report →
- X-Linked Lymphoproliferative Disease and XMENReads 2 of these genesSH2D1AXIAPAbout this report →
- Hereditary Optic NeuropathyReads 4 of these genesMT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 4 of these genesCPT1ACPT2SLC25A20ACAD9About this report →
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- Hereditary Leiomyomatosis and Renal Cell CancerReads 1 of these genesFHAbout this report →
- Johanson-Blizzard SyndromeReads 1 of these genesUBR1About this report →
- Lysosomal Acid Lipase Deficiency (Wolman Disease and CESD)Reads 1 of these genesLIPAAbout this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- Familial Intrahepatic CholestasisReads 3 of these genesNR1H4PSKH1TJP2About this report →
- Primary Mitochondrial DiseaseReads 10 of these genesDGUOKMRM2TFAMCOX16GFM1MPV17About this report →
- Alagille SyndromeReads 1 of these genesJAG1About this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Rare Inherited Coagulation Factor DeficienciesReads 2 of these genesF13A1F13BAbout this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7BAbout this report →
- HaemophiliaReads 1 of these genesF8About this report →
- Hereditary Fructose Intolerance & Gluconeogenesis DefectsReads 1 of these genesPCK1About this report →
- TyrosinemiaReads 1 of these genesFAHAbout this report →
- Lysosomal Storage DiseaseReads 4 of these genesLIPASMPD1ASAH1GBA1About this report →
- Glycogen Storage DiseaseReads 2 of these genesSLC2A2GBE1About this report →
- GalactosemiaReads 1 of these genesGALTAbout this report →
- Maple Syrup Urine DiseaseReads 1 of these genesDLDAbout this report →
- MelanomaReads 1 of these genesPOT1About this report →
- Noonan SyndromeReads 2 of these genesMAP2K1NRASAbout this report →
- Bardet-Biedl and Alström SyndromesReads 2 of these genesALMS1IFT172About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesACTG2About this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 1 of these genesAMACRAbout this report →
- Surfactant Metabolism DysfunctionReads 1 of these genesMARS1About this report →
- Congenital Disorders of GlycosylationReads 4 of these genesPIGAVMA22COG4MPIAbout this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesIFT122About this report →
- Hereditary HypolipoproteinemiasReads 1 of these genesAPOA1About this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesDEF6About this report →
- Diabetes MellitusReads 2 of these genesMT-TL1SLC2A2About this report →
- Hepatic Porphyria DisordersReads 1 of these genesFECHAbout this report →
- Other Inborn Errors of ImmunityReads 5 of these genesDEF6IL21RSH2D1AXIAPSKIC3About this report →
- Charcot-Marie-Tooth DiseaseReads 3 of these genesMARS1MPV17JAG1About this report →
- PorphyriaReads 1 of these genesFECHAbout this report →
- Pyruvate Dehydrogenase & Pyruvate Carboxylase DeficiencyReads 1 of these genesDLDAbout this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 1 of these genesIL12RB1About this report →
- Epilepsy (Full Panel)Reads 4 of these genesPIGAEPM2ANHLRC1SCARB2About this report →
- Hereditary AmyloidosisReads 1 of these genesAPOA1About this report →
- Myofibrillar MyopathiesReads 1 of these genesRYR1About this report →
- OsteopetrosisReads 1 of these genesOSTM1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesPEX6SCYL1About this report →
- Parkinson DiseaseReads 1 of these genesGBA1About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesMAP2K1NRASAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Congenital MyopathiesReads 1 of these genesRYR1About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGAAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesSLC2A2About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesDCDC2About this report →
- Syndromic CraniosynostosisReads 1 of these genesIFT122About this report →
- Inherited IchthyosesReads 1 of these genesCLDN1About this report →
- Intellectual DisabilityReads 3 of these genesMED12SMAD4ATRXAbout this report →
- VitreoretinopathyReads 1 of these genesCTC1About this report →
- Spinal Muscular AtrophyReads 1 of these genesASAH1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesTNPO3About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesSKIC3About this report →
- DNA Repair DiseaseReads 1 of these genesAPTXAbout this report →
- Female InfertilityReads 1 of these genesGALTAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesCYP7B1About this report →
- Retinitis PigmentosaReads 1 of these genesIFT172About this report →
Les genene knyttet til Liver failure, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test141 gener knyttet til Liver failure
Endringer i disse genene forårsaker sjeldne tilstander der Liver failure 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 |
|---|---|---|
| ABCD3ATP binding cassette subfamily D member 3 | Alltid | I 1 tilstand |
| APOA1apolipoprotein A1 | Alltid | I 1 tilstand |
| ATP7BATPase copper transporting beta | Alltid | I 1 tilstand |
| CYP7B1cytochrome P450 family 7 subfamily B member 1 | Alltid | I 2 tilstander |
| DCDC2doublecortin domain containing 2 | Alltid | I 1 tilstand |
| DGUOKdeoxyguanosine kinase | Alltid | I 1 tilstand |
| F8coagulation factor VIII | Alltid | I 1 tilstand |
| FAHfumarylacetoacetate hydrolase | Alltid | I 1 tilstand |
| FHfumarate hydratase | Alltid | I 1 tilstand |
| IL18BPinterleukin 18 binding protein | Alltid | I 1 tilstand |
| IL27RAinterleukin 27 receptor subunit alpha | Alltid | I 1 tilstand |
| LIPAlipase A, lysosomal acid type | Alltid | I 3 tilstander |
| MARS1methionyl-tRNA synthetase 1 | Alltid | I 1 tilstand |
| MRM2mitochondrial rRNA methyltransferase 2 | Alltid | I 1 tilstand |
| NR1H4nuclear receptor subfamily 1 group H member 4 | Alltid | I 1 tilstand |
| PCK1phosphoenolpyruvate carboxykinase 1 | Alltid | I 1 tilstand |
| PEX19peroxisomal biogenesis factor 19 | Alltid | I 2 tilstander |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Alltid | I 2 tilstander |
| POT1protection of telomeres 1 | Alltid | I 1 tilstand |
| PSKH1protein serine kinase H1 | Alltid | I 1 tilstand |
| RFC4replication factor C subunit 4 | Alltid | I 1 tilstand |
| TFAMtranscription factor A, mitochondrial | Alltid | I 1 tilstand |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Alltid | I 1 tilstand |
| CPT1Acarnitine palmitoyltransferase 1A | Svært ofte (80–99 %) | I 1 tilstand |
| OTCornithine transcarbamylase | Svært ofte (80–99 %) | I 1 tilstand |
| PEX1peroxisomal biogenesis factor 1 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX10peroxisomal biogenesis factor 10 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX11Bperoxisomal biogenesis factor 11 beta | Svært ofte (80–99 %) | I 1 tilstand |
| PEX12peroxisomal biogenesis factor 12 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX13peroxisomal biogenesis factor 13 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX14peroxisomal biogenesis factor 14 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX16peroxisomal biogenesis factor 16 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX2peroxisomal biogenesis factor 2 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX26peroxisomal biogenesis factor 26 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX3peroxisomal biogenesis factor 3 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX5peroxisomal biogenesis factor 5 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX6peroxisomal biogenesis factor 6 | Svært ofte (80–99 %) | I 1 tilstand |
| SMPD1sphingomyelin phosphodiesterase 1 | Svært ofte (80–99 %) | I 2 tilstander |
| ACTG2actin gamma 2, smooth muscle | Ofte (30–79 %) | I 1 tilstand |
| AKR1D1aldo-keto reductase family 1 member D1 | Ofte (30–79 %) | I 2 tilstander |
Vis 101 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| COX16cytochrome c oxidase assembly factor COX16 | Ofte (30–79 %) | I 1 tilstand |
| CPT2carnitine palmitoyltransferase 2 | Ofte (30–79 %) | I 2 tilstander |
| DEF6DEF6 guanine nucleotide exchange factor | Ofte (30–79 %) | I 1 tilstand |
| FOCADfocadhesin | Ofte (30–79 %) | I 1 tilstand |
| GALTgalactose-1-phosphate uridylyltransferase | Ofte (30–79 %) | I 1 tilstand |
| GFM1G elongation factor mitochondrial 1 | Ofte (30–79 %) | I 1 tilstand |
| H4C3H4 clustered histone 3 | Ofte (30–79 %) | I 1 tilstand |
| IL12Ainterleukin 12A | Ofte (30–79 %) | I 1 tilstand |
| IL12RB1interleukin 12 receptor subunit beta 1 | Ofte (30–79 %) | I 1 tilstand |
| IRF5interferon regulatory factor 5 | Ofte (30–79 %) | I 1 tilstand |
| MMEL1membrane metalloendopeptidase like 1 | Ofte (30–79 %) | I 1 tilstand |
| MPV17mitochondrial inner membrane protein MPV17 | Ofte (30–79 %) | I 1 tilstand |
| MRPS7mitochondrial ribosomal protein S7 | Ofte (30–79 %) | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Ofte (30–79 %) | I 1 tilstand |
| POU2AF1POU class 2 homeobox associating factor 1 | Ofte (30–79 %) | I 1 tilstand |
| RBM10RNA binding motif protein 10 | Ofte (30–79 %) | I 1 tilstand |
| SC5Dsterol-C5-desaturase | Ofte (30–79 %) | I 1 tilstand |
| SERAC1serine active site containing 1 | Ofte (30–79 %) | I 1 tilstand |
| SLC7A7solute carrier family 7 member 7 | Ofte (30–79 %) | I 1 tilstand |
| SPIBSpi-B transcription factor | Ofte (30–79 %) | I 1 tilstand |
| TJP2tight junction protein 2 | Ofte (30–79 %) | I 1 tilstand |
| TNFSF15TNF superfamily member 15 | Ofte (30–79 %) | I 1 tilstand |
| TNPO3transportin 3 | Ofte (30–79 %) | I 1 tilstand |
| VMA22vacuolar ATPase assembly factor VMA22 | Ofte (30–79 %) | I 1 tilstand |
| ACDACD shelterin complex subunit and telomerase recruitment factor | Noen ganger (5–29 %) | I 1 tilstand |
| ACVRL1activin A receptor like type 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ALMS1ALMS1 centrosome and basal body associated protein | Noen ganger (5–29 %) | I 1 tilstand |
| ASLargininosuccinate lyase | Noen ganger (5–29 %) | I 1 tilstand |
| BAATbile acid-CoA:amino acid N-acyltransferase | Noen ganger (5–29 %) | I 1 tilstand |
| BTNL2butyrophilin like 2 | Noen ganger (5–29 %) | I 1 tilstand |
| CILK1ciliogenesis associated kinase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| CLDN1claudin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| COG4component of oligomeric golgi complex 4 | Noen ganger (5–29 %) | I 1 tilstand |
| CTC1CST telomere replication complex component 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DKC1dyskerin pseudouridine synthase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DLDdihydrolipoamide dehydrogenase | Noen ganger (5–29 %) | I 1 tilstand |
| ENGendoglin | Noen ganger (5–29 %) | I 1 tilstand |
| EPM2AEPM2A glucan phosphatase, laforin | Noen ganger (5–29 %) | I 2 tilstander |
| GDF2growth differentiation factor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| HLA-Bmajor histocompatibility complex, class I, B | Noen ganger (5–29 %) | I 1 tilstand |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Noen ganger (5–29 %) | I 2 tilstander |
| IARS1isoleucyl-tRNA synthetase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Noen ganger (5–29 %) | I 1 tilstand |
| IL21Rinterleukin 21 receptor | Noen ganger (5–29 %) | I 1 tilstand |
| JAG1jagged canonical Notch ligand 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MED12mediator complex subunit 12 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND3mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Noen ganger (5–29 %) | I 1 tilstand |
| NHLRC1NHL repeat containing E3 ubiquitin protein ligase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| NHP2NHP2 ribonucleoprotein | Noen ganger (5–29 %) | I 1 tilstand |
| NOP10NOP10 ribonucleoprotein | Noen ganger (5–29 %) | I 1 tilstand |
| NPM1nucleophosmin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PARNpoly(A)-specific ribonuclease | Noen ganger (5–29 %) | I 1 tilstand |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Noen ganger (5–29 %) | I 1 tilstand |
| RTEL1regulator of telomere elongation helicase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SH2D1ASH2 domain containing 1A | Noen ganger (5–29 %) | I 1 tilstand |
| SLC25A20solute carrier family 25 member 20 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC2A2solute carrier family 2 member 2 | Noen ganger (5–29 %) | I 1 tilstand |
| SMAD4SMAD family member 4 | Noen ganger (5–29 %) | I 1 tilstand |
| TERCtelomerase RNA component | Noen ganger (5–29 %) | I 1 tilstand |
| TERTtelomerase reverse transcriptase | Noen ganger (5–29 %) | I 1 tilstand |
| TINF2TERF1 interacting nuclear factor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| TYMSthymidylate synthetase | Noen ganger (5–29 %) | I 1 tilstand |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| WRAP53WD repeat containing antisense to TP53 | Noen ganger (5–29 %) | I 1 tilstand |
| XIAPX-linked inhibitor of apoptosis | Noen ganger (5–29 %) | I 2 tilstander |
| ASAH1N-acylsphingosine amidohydrolase 1 | Sjelden (1–4%) | I 1 tilstand |
| ATRXATRX chromatin remodeler | Sjelden (1–4%) | I 1 tilstand |
| F13A1coagulation factor XIII A chain | Sjelden (1–4%) | I 1 tilstand |
| F13Bcoagulation factor XIII B chain | Sjelden (1–4%) | I 1 tilstand |
| GBA1glucosylceramidase beta 1 | Sjelden (1–4%) | I 2 tilstander |
| MAP2K1mitogen-activated protein kinase kinase 1 | Sjelden (1–4%) | I 1 tilstand |
| NRASNRAS proto-oncogene, GTPase | Sjelden (1–4%) | I 1 tilstand |
| RYR1ryanodine receptor 1 | Sjelden (1–4%) | I 1 tilstand |
| SCARB2scavenger receptor class B member 2 | Sjelden (1–4%) | I 1 tilstand |
| SLC25A15solute carrier family 25 member 15 | Sjelden (1–4%) | I 1 tilstand |
| ACAD9acyl-CoA dehydrogenase family member 9 | Ikke registrert | I 1 tilstand |
| AMACRalpha-methylacyl-CoA racemase | Ikke registrert | I 1 tilstand |
| APTXaprataxin | Ikke registrert | I 1 tilstand |
| COQ2coenzyme Q2, polyprenyltransferase | Ikke registrert | I 1 tilstand |
| FECHferrochelatase | Ikke registrert | I 1 tilstand |
| GBE11,4-alpha-glucan branching enzyme 1 | Ikke registrert | I 1 tilstand |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Ikke registrert | I 1 tilstand |
| IFT122intraflagellar transport 122 | Ikke registrert | I 1 tilstand |
| IFT172intraflagellar transport 172 | Ikke registrert | I 1 tilstand |
| MPImannose phosphate isomerase | Ikke registrert | I 1 tilstand |
| NDUFS4NADH:ubiquinone oxidoreductase subunit S4 | Ikke registrert | I 1 tilstand |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Ikke registrert | I 1 tilstand |
| PCK2phosphoenolpyruvate carboxykinase 2, mitochondrial | Ikke registrert | I 1 tilstand |
| SCYL1SCY1 like pseudokinase 1 | Ikke registrert | I 1 tilstand |
| SKIC3SKI3 subunit of superkiller complex | 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.
Smalere egenskaper
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 2026.10.17-8666dff2.
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Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 470+ physician-ready reports.
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