AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Trait
Peritonitis
Inflammation of the peritoneum.
Summary
- Also called
- Inflammation of the peritoneum
AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
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/peritonitis.json"
page <- fromJSON(url)
page$trait$namePeritonitisHP:0002586
AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Read the genes linked to Peritonitis, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test23 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.
- Nephrotic SyndromeReads 19 of these genesACTN4ARHGDIACOQ8BDAAM2EMP2KANK2About this report →
- Focal Segmental GlomerulosclerosisReads 9 of these genesACTN4ANLNAPOL1CD2APCRB2INF2About this report →
- GlomerulosclerosisReads 7 of these genesACTN4ANLNCRB2INF2MYO1EPAX2About this report →
- Familial Mediterranean FeverReads 1 of these genesMEFVAbout this report →
Show 19 more reports
- Hereditary Periodic Fever SyndromesReads 2 of these genesMVKTNFRSF1AAbout this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 1 of these genesBRCA1About this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- Alport SyndromeReads 1 of these genesCOL4A3About this report →
- PorokeratosisReads 1 of these genesMVKAbout this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF2About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesMYH11About this report →
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 1 of these genesCFBAbout this report →
- ThrombophiliaReads 1 of these genesF5About this report →
- Rare Inherited Coagulation Factor DeficienciesReads 1 of these genesF5About this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesPAX2About this report →
- Severe Congenital NeutropeniaReads 1 of these genesELANEAbout this report →
- Aortic AneurysmReads 1 of these genesMYH11About this report →
- Fanconi AnemiaReads 1 of these genesBRCA1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesWT1About this report →
- DNA Repair DiseaseReads 1 of these genesBRCA1About this report →
- Female InfertilityReads 1 of these genesNUP107About this report →
- Other Inborn Errors of ImmunityReads 2 of these genesNCF2CFBAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesINF2About this report →
Read the genes linked to Peritonitis, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test47 genes linked to Peritonitis
Changes in these genes cause rare conditions in which Peritonitis 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 |
|---|---|---|
| MYH11myosin heavy chain 11 | Always | In 1 condition |
| BRCA1BRCA1 DNA repair associated | Very often (80–99%) | In 1 condition |
| MEFVMEFV innate immunity regulator, pyrin | Very often (80–99%) | In 3 conditions |
| CALRcalreticulin | Sometimes (5–29%) | In 1 condition |
| F5coagulation factor V | Sometimes (5–29%) | In 1 condition |
| FOCADfocadhesin | Sometimes (5–29%) | In 1 condition |
| JAK2Janus kinase 2 | Sometimes (5–29%) | In 1 condition |
| MVKmevalonate kinase | Sometimes (5–29%) | In 1 condition |
| NCF2neutrophil cytosolic factor 2 | Sometimes (5–29%) | In 1 condition |
| TNFRSF1ATNF receptor superfamily member 1A | Sometimes (5–29%) | In 1 condition |
| TRAF3TNF receptor associated factor 3 | Sometimes (5–29%) | In 1 condition |
| ACTN4actinin alpha 4 | Rarely (1–4%) | In 1 condition |
| ANKFY1ankyrin repeat and FYVE domain containing 1 | Rarely (1–4%) | In 1 condition |
| ANLNanillin, actin binding protein | Rarely (1–4%) | In 1 condition |
| APOL1apolipoprotein L1 | Rarely (1–4%) | In 1 condition |
| ARHGAP24Rho GTPase activating protein 24 | Rarely (1–4%) | In 1 condition |
| ARHGDIARho GDP dissociation inhibitor alpha | Rarely (1–4%) | In 1 condition |
| AVILadvillin | Rarely (1–4%) | In 1 condition |
| CD2APCD2 associated protein | Rarely (1–4%) | In 1 condition |
| COL4A3collagen type IV alpha 3 chain | Rarely (1–4%) | In 1 condition |
| COQ8Bcoenzyme Q8B | Rarely (1–4%) | In 1 condition |
| CRB2crumbs cell polarity complex component 2 | Rarely (1–4%) | In 1 condition |
| DAAM2dishevelled associated activator of morphogenesis 2 | Rarely (1–4%) | In 1 condition |
| ELANEelastase, neutrophil expressed | Rarely (1–4%) | In 1 condition |
| EMP2epithelial membrane protein 2 | Rarely (1–4%) | In 1 condition |
| GAPVD1GTPase activating protein and VPS9 domains 1 | Rarely (1–4%) | In 1 condition |
| INF2inverted formin 2 | Rarely (1–4%) | In 1 condition |
| KANK2KN motif and ankyrin repeat domains 2 | Rarely (1–4%) | In 1 condition |
| LAMA5laminin subunit alpha 5 | Rarely (1–4%) | In 1 condition |
| MAGI2membrane associated guanylate kinase, WW and PDZ domain containing 2 | Rarely (1–4%) | In 1 condition |
| MYO1Emyosin IE | Rarely (1–4%) | In 1 condition |
| NPHS1NPHS1 adhesion molecule, nephrin | Rarely (1–4%) | In 1 condition |
| NPHS2NPHS2 stomatin family member, podocin | Rarely (1–4%) | In 1 condition |
| NUP107nucleoporin 107 | Rarely (1–4%) | In 1 condition |
| NUP133nucleoporin 133 | Rarely (1–4%) | In 1 condition |
| NUP160nucleoporin 160 | Rarely (1–4%) | In 1 condition |
| NUP205nucleoporin 205 | Rarely (1–4%) | In 1 condition |
| NUP37nucleoporin 37 | Rarely (1–4%) | In 1 condition |
| NUP85nucleoporin 85 | Rarely (1–4%) | In 1 condition |
| NUP93nucleoporin 93 | Rarely (1–4%) | In 1 condition |
Show 7 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| PAX2paired box 2 | Rarely (1–4%) | In 1 condition |
| PLCE1phospholipase C epsilon 1 | Rarely (1–4%) | In 1 condition |
| PTPROprotein tyrosine phosphatase receptor type O | Rarely (1–4%) | In 1 condition |
| TBC1D8BTBC1 domain family member 8B | Rarely (1–4%) | In 1 condition |
| TRPC6transient receptor potential cation channel subfamily C member 6 | Rarely (1–4%) | In 1 condition |
| WT1WT1 transcription factor | Rarely (1–4%) | In 1 condition |
| CFBcomplement factor B | 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.
Narrower traits
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-e609d43e.
AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
From traits to your genome
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.
From $449
Free shipping · Results in 6–8 weeks
