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Trait
Liver inflammation
Clinical name: Hepatitis
Inflammation of the liver.
Summary
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This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/hepatitis.json"
page <- fromJSON(url)
page$trait$nameLiver inflammationHP:0012115
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Get my Genome Test54 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.
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 9 of these genesBLNKBTKCD79ACD79BIGHMIGLL1About this report →
- Other Inborn Errors of ImmunityReads 29 of these genesIRF4SPINK5TPP2XIAPARPC5BLNKAbout this report →
- Chronic Mucocutaneous CandidiasisReads 4 of these genesIL17RAIL17RCSTAT1TRAF3IP2About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 2 of these genesPIK3CDPIK3R1About this report →
Show 50 more reports
- Autoimmune DiseaseReads 6 of these genesAIRECASP10FASFASLGFOXP3STAT1About this report →
- Disorder of Copper MetabolismReads 2 of these genesATP7BATP7AAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 3 of these genesCASP10FASFASLGAbout this report →
- Alpha-1 Antitrypsin DeficiencyReads 1 of these genesSERPINA1About this report →
- Autoimmune Polyendocrine Syndrome Type 1 (APECED)Reads 1 of these genesAIREAbout this report →
- CYP7B1-Related Spastic Paraplegia and Liver DiseaseReads 1 of these genesCYP7B1About this report →
- ITCH DeficiencyReads 1 of these genesITCHAbout this report →
- Mucopolysaccharidosis Type VII (Sly Syndrome)Reads 1 of these genesGUSBAbout this report →
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- Congenital Intestinal Atresia & Short BowelReads 1 of these genesTTC7AAbout this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT1About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 2 of these genesIL12RB1STAT1About this report →
- Type I InterferonopathiesReads 2 of these genesACP5IFIH1About this report →
- X-Linked Lymphoproliferative Disease and XMENReads 1 of these genesXIAPAbout this report →
- Severe Combined ImmunodeficiencyReads 3 of these genesCD247CD3DCD3EAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 3 of these genesOTULINACP5IFIH1About this report →
- Hyper-IgM SyndromesReads 1 of these genesCD40LGAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesGNASAbout this report →
- Neonatal Diabetes MellitusReads 2 of these genesNEUROG3GLIS3About this report →
- Hyper-IgE SyndromeReads 1 of these genesSPINK5About this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesFOXP3About this report →
- Diabetes MellitusReads 2 of these genesNEUROG3GLIS3About this report →
- Thyroid CancerReads 2 of these genesAIREGNASAbout this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesIFIH1About this report →
- Red Blood Cell Membrane DisordersReads 1 of these genesPIEZO1About this report →
- Coffin-Siris SyndromeReads 1 of these genesARID2About this report →
- Urea Cycle DisorderReads 1 of these genesSLC25A15About this report →
- Congenital Diarrhoeas & EnteropathiesReads 1 of these genesNEUROG3About this report →
- Cutis LaxaReads 1 of these genesATP7AAbout this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesPIEZO1About this report →
- Inherited Complement and Properdin DeficienciesReads 1 of these genesC1SAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesC1SAbout this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesALMS1About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesCOG6PGM1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesTBX19About this report →
- Spinal Muscular AtrophyReads 1 of these genesATP7AAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesTNPO3About this report →
- Osteogenesis ImperfectaReads 1 of these genesIFIH1About this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesATP7AIFIH1CYP7B1About this report →
- Dilated CardiomyopathyReads 1 of these genesPGM1About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesTBX19About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGUSBAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesCYP7B1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesATP7AAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesIFIH1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesATP7AAbout this report →
- Intellectual DisabilityReads 1 of these genesTCF4About this report →
Read the genes linked to Liver inflammation, and the rest of your genome, with one test.
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Get my Genome Test71 genes linked to Liver inflammation
Changes in these genes cause rare conditions in which Liver inflammation is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ARID2AT-rich interaction domain 2 | Always | In 1 condition |
| CILK1ciliogenesis associated kinase 1 | Always | In 1 condition |
| IL27RAinterleukin 27 receptor subunit alpha | Always | In 1 condition |
| IRF4interferon regulatory factor 4 | Always | In 1 condition |
| NEUROG3neurogenin 3 | Always | In 1 condition |
| OTULINOTU deubiquitinase with linear linkage specificity | Always | In 1 condition |
| RC3H1ring finger and CCCH-type domains 1 | Always | In 1 condition |
| SPINK5serine peptidase inhibitor Kazal type 5 | Always | In 1 condition |
| ATP7BATPase copper transporting beta | Very often (80–99%) | In 1 condition |
| CYP7A1cytochrome P450 family 7 subfamily A member 1 | Very often (80–99%) | In 1 condition |
| TPP2tripeptidyl peptidase 2 | Very often (80–99%) | In 1 condition |
| XIAPX-linked inhibitor of apoptosis | Very often (80–99%) | In 2 conditions |
| ARPC5actin related protein 2/3 complex subunit 5 | Often (30–79%) | In 1 condition |
| ATP7AATPase copper transporting alpha | Often (30–79%) | In 1 condition |
| GUSBglucuronidase beta | Often (30–79%) | In 1 condition |
| ITCHitchy E3 ubiquitin protein ligase | Often (30–79%) | In 2 conditions |
| SERPINA1serpin family A member 1 | Often (30–79%) | In 1 condition |
| SHPKsedoheptulokinase | Often (30–79%) | In 1 condition |
| SLC25A15solute carrier family 25 member 15 | Often (30–79%) | In 1 condition |
| ACP5acid phosphatase 5, tartrate resistant | Sometimes (5–29%) | In 1 condition |
| AIREautoimmune regulator | Sometimes (5–29%) | In 1 condition |
| ALMS1ALMS1 centrosome and basal body associated protein | Sometimes (5–29%) | In 1 condition |
| BLNKB cell linker | Sometimes (5–29%) | In 1 condition |
| BTKBruton tyrosine kinase | Sometimes (5–29%) | In 1 condition |
| CASP10caspase 10 | Sometimes (5–29%) | In 1 condition |
| CD247CD247 molecule | Sometimes (5–29%) | In 1 condition |
| CD3DCD3 delta subunit of T-cell receptor complex | Sometimes (5–29%) | In 1 condition |
| CD3ECD3 epsilon subunit of T-cell receptor complex | Sometimes (5–29%) | In 1 condition |
| CD40LGCD40 ligand | Sometimes (5–29%) | In 1 condition |
| CD79ACD79a molecule | Sometimes (5–29%) | In 1 condition |
| CD79BCD79b molecule | Sometimes (5–29%) | In 1 condition |
| CLEC7AC-type lectin domain containing 7A | Sometimes (5–29%) | In 1 condition |
| COG6component of oligomeric golgi complex 6 | Sometimes (5–29%) | In 1 condition |
| FASFas cell surface death receptor | Sometimes (5–29%) | In 1 condition |
| FASLGFas ligand | Sometimes (5–29%) | In 1 condition |
| FOXP3forkhead box P3 | Sometimes (5–29%) | In 2 conditions |
| GPR35G protein-coupled receptor 35 | Sometimes (5–29%) | In 1 condition |
| IFIH1interferon induced with helicase C domain 1 | Sometimes (5–29%) | In 1 condition |
| IGHMimmunoglobulin heavy constant mu | Sometimes (5–29%) | In 1 condition |
| IGLL1immunoglobulin lambda like polypeptide 1 | Sometimes (5–29%) | In 1 condition |
Show 31 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| IL12Ainterleukin 12A | Sometimes (5–29%) | In 1 condition |
| IL12RB1interleukin 12 receptor subunit beta 1 | Sometimes (5–29%) | In 1 condition |
| IL17Finterleukin 17F | Sometimes (5–29%) | In 1 condition |
| IL17RAinterleukin 17 receptor A | Sometimes (5–29%) | In 1 condition |
| IL17RCinterleukin 17 receptor C | Sometimes (5–29%) | In 1 condition |
| IRF5interferon regulatory factor 5 | Sometimes (5–29%) | In 1 condition |
| LRRC8Aleucine rich repeat containing 8 VRAC subunit A | Sometimes (5–29%) | In 1 condition |
| MMEL1membrane metalloendopeptidase like 1 | Sometimes (5–29%) | In 1 condition |
| MST1macrophage stimulating 1 | Sometimes (5–29%) | In 1 condition |
| PGM1phosphoglucomutase 1 | Sometimes (5–29%) | In 1 condition |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Sometimes (5–29%) | In 1 condition |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Sometimes (5–29%) | In 1 condition |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sometimes (5–29%) | In 1 condition |
| POU2AF1POU class 2 homeobox associating factor 1 | Sometimes (5–29%) | In 1 condition |
| SEMA4Dsemaphorin 4D | Sometimes (5–29%) | In 1 condition |
| SPI1Spi-1 proto-oncogene | Sometimes (5–29%) | In 1 condition |
| SPIBSpi-B transcription factor | Sometimes (5–29%) | In 1 condition |
| STAT1signal transducer and activator of transcription 1 | Sometimes (5–29%) | In 1 condition |
| SYKspleen associated tyrosine kinase | Sometimes (5–29%) | In 1 condition |
| TBX19T-box transcription factor 19 | Sometimes (5–29%) | In 1 condition |
| TCF3transcription factor 3 | Sometimes (5–29%) | In 1 condition |
| TCF4transcription factor 4 | Sometimes (5–29%) | In 1 condition |
| TNFSF15TNF superfamily member 15 | Sometimes (5–29%) | In 1 condition |
| TNPO3transportin 3 | Sometimes (5–29%) | In 1 condition |
| TRAF3IP2TRAF3 interacting protein 2 | Sometimes (5–29%) | In 1 condition |
| GNASGNAS complex locus | Rarely (1–4%) | In 1 condition |
| PI4KAphosphatidylinositol 4-kinase alpha | Rarely (1–4%) | In 1 condition |
| TTC7Atetratricopeptide repeat domain 7A | Rarely (1–4%) | In 1 condition |
| C1Scomplement C1s | Not recorded | In 1 condition |
| CYP7B1cytochrome P450 family 7 subfamily B member 1 | Not recorded | In 1 condition |
| GLIS3GLIS family zinc finger 3 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
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Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.18-8b139e39.
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