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PrisijungtiKlaustiSekvenuokite savo genomą↗
Požymis
Chronic diarrhea
The presence of chronic diarrhea, which is usually taken to mean diarrhea that has persisted for over 4 weeks.
Santrauka
- Taip pat vadinama
- Diarrhea, recurrent, Recurrent diarrhea, Chronic diarrhoea
- Kūno sistema
- Abnormality of the digestive system
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/chronic-diarrhea.json"
page <- fromJSON(url)
page$trait$nameChronic diarrheaHP:0002028
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Chronic diarrhea, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test81 condition report reads 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.
- Other Inborn Errors of ImmunityReads 49 of these genesADAATP6AP1B2MBACH2CD3GCR2About this report →
- Severe Combined ImmunodeficiencyReads 14 of these genesADADCLRE1CJAK3IL2RGIL7RNUDCD3About this report →
- IPEX Syndrome and Other TregopathiesReads 4 of these genesBACH2FOXP3IL2RALRBAAbout this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 2 of these genesPIK3CDPIK3R1About this report →
Show 77 more reports
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 2 of these genesALKPHOX2BAbout this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 4 of these genesTCF3BTKIGHMPIK3R1About this report →
- EBV-Driven Lymphoproliferation and CARD11 Immune DysregulationReads 2 of these genesIKZF2CARD11About this report →
- Leukocyte Adhesion DeficiencyReads 2 of these genesITGB2SLC35C1About this report →
- Congenital Diarrhoeas & EnteropathiesReads 4 of these genesGUCY2CSLC5A1STX3EPCAMAbout this report →
- ARC Syndrome 1 (VPS33B)Reads 1 of these genesVPS33BAbout this report →
- ARC Syndrome 2 (VIPAS39)Reads 1 of these genesVIPAS39About this report →
- Ataxia-TelangiectasiaReads 1 of these genesATMAbout this report →
- Cerebrotendinous XanthomatosisReads 1 of these genesCYP27A1About this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- Congenital Central Hypoventilation SyndromeReads 1 of these genesPHOX2BAbout this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- Glucose-Galactose MalabsorptionReads 1 of these genesSLC5A1About this report →
- Hao-Fountain SyndromeReads 1 of these genesUSP7About this report →
- ITCH DeficiencyReads 1 of these genesITCHAbout this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- Polyglucosan Body Myopathy 1 (RBCK1)Reads 1 of these genesRBCK1About this report →
- Saul-Wilson SyndromeReads 1 of these genesCOG4About this report →
- X-linked Autoinflammatory DiseaseReads 1 of these genesIKBKGAbout this report →
- ZTTK SyndromeReads 1 of these genesSONAbout this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 3 of these genesCR2IRF2BP2LRBAAbout this report →
- Hereditary Periodic Fever SyndromesReads 2 of these genesMVKTNFRSF1AAbout this report →
- Hyper-IgE SyndromeReads 2 of these genesIL6STSPINK5About this report →
- Acrodermatitis EnteropathicaReads 1 of these genesSLC39A4About this report →
- Congenital Intestinal Atresia & Short BowelReads 1 of these genesCLMPAbout this report →
- Hereditary FibromatosesReads 1 of these genesANTXR2About this report →
- Sandhoff Disease and GM2 Activator DeficiencyReads 1 of these genesHEXBAbout this report →
- Tubular Aggregate MyopathyReads 1 of these genesORAI1About this report →
- Wiskott-Aldrich Syndrome SpectrumReads 1 of these genesWASAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 4 of these genesSKIC2PSMB10OTULINPOLA1About this report →
- Autoimmune DiseaseReads 3 of these genesFOXP3ZAP70CASP8About this report →
- Congenital Disorders of GlycosylationReads 6 of these genesATP6AP1ALG1COG6COG4PGM1SLC35C1About this report →
- Severe Congenital NeutropeniaReads 2 of these genesVPS45WASAbout this report →
- Type I InterferonopathiesReads 2 of these genesPSMB10POLA1About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesPHOX2BAbout this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRMRPAbout this report →
- Myelodysplastic Syndrome (MDS)Reads 1 of these genesSAMD9About this report →
- Lysosomal Storage DiseaseReads 4 of these genesCYP27A1IDUAASAH1HEXBAbout this report →
- Inherited Predisposition to Myeloid Blood CancersReads 1 of these genesSAMD9About this report →
- PorokeratosisReads 1 of these genesMVKAbout this report →
- Ectodermal DysplasiasReads 2 of these genesNFKBIAIKBKGAbout this report →
- DNA Repair DiseaseReads 3 of these genesDCLRE1CNBNERCC2About this report →
- Lynch SyndromeReads 1 of these genesEPCAMAbout this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesSTAT5BAbout this report →
- Spinal Muscular AtrophyReads 2 of these genesATP7AASAH1About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesCASP8About this report →
- Hereditary HypolipoproteinemiasReads 1 of these genesMTTPAbout this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesTERTAbout this report →
- Inherited Neurodegenerative DisordersReads 7 of these genesATMATP7ACYP27A1HACE1MTTPASAH1About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNDC1About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 1 of these genesATMAbout this report →
- Familial Pulmonary FibrosisReads 1 of these genesTERTAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 5 of these genesATP7ACYP27A1ETHE1MTTPHEXBAbout this report →
- Hereditary AmyloidosisReads 1 of these genesB2MAbout this report →
- Diamond-Blackfan AnemiaReads 1 of these genesHEATR3About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesCYP27A1MTTPAbout this report →
- Intellectual DisabilityReads 4 of these genesPOLA1ADNPKMT5BPPP2R5DAbout this report →
- Cutis LaxaReads 1 of these genesATP7AAbout this report →
- Epidermolysis BullosaReads 1 of these genesPKP1About this report →
- Neonatal Diabetes MellitusReads 1 of these genesIL2RAAbout this report →
- Dyskeratosis CongenitaReads 1 of these genesTERTAbout this report →
- VitreoretinopathyReads 1 of these genesIKBKGAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesERCC2About this report →
- Diabetes MellitusReads 1 of these genesIL2RAAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesWASAbout this report →
- Primary Mitochondrial DiseaseReads 2 of these genesATP5F1AMGME1About this report →
- Dilated CardiomyopathyReads 1 of these genesPGM1About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesCHD7About this report →
- Female InfertilityReads 1 of these genesATMAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesHACE1About this report →
- Leigh SyndromeReads 1 of these genesETHE1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesATP7AAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesCYP27A1About this report →
- Hearing Loss and DeafnessReads 1 of these genesIKZF2About this report →
- Epilepsy (Full Panel)Reads 1 of these genesHACE1About this report →
Vienu tyrimu sužinokite genus, susijusius su Chronic diarrhea, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test124 genų susiję su Chronic diarrhea
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Chronic diarrhea. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| ADAadenosine deaminase | Visada | 2 ligose |
| ATP6AP1ATPase H+ transporting accessory protein 1 | Visada | 1 ligoje |
| B2Mbeta-2-microglobulin | Visada | 1 ligoje |
| BACH2BACH transcriptional regulator 2 | Visada | 1 ligoje |
| CARD8caspase recruitment domain family member 8 | Visada | 1 ligoje |
| CD3GCD3 gamma subunit of T-cell receptor complex | Visada | 1 ligoje |
| CHASERRCHD2 adjacent suppressive regulatory RNA | Visada | 1 ligoje |
| CLMPCXADR like cell adhesion molecule | Visada | 1 ligoje |
| CR2complement C3d receptor 2 | Visada | 1 ligoje |
| DCLRE1CDNA cross-link repair 1C | Visada | 2 ligose |
| DNASE2deoxyribonuclease 2, lysosomal | Visada | 1 ligoje |
| FLT3LGfms related receptor tyrosine kinase 3 ligand | Visada | 1 ligoje |
| FOXP3forkhead box P3 | Visada | 1 ligoje |
| GUCY2Cguanylate cyclase 2C | Visada | 2 ligose |
| HYOU1hypoxia up-regulated 1 | Visada | 1 ligoje |
| IGKCimmunoglobulin kappa constant | Visada | 1 ligoje |
| IKZF2IKAROS family zinc finger 2 | Visada | 1 ligoje |
| IL2RAinterleukin 2 receptor subunit alpha | Visada | 1 ligoje |
| IL6STinterleukin 6 cytokine family signal transducer | Visada | 1 ligoje |
| ITGB2integrin subunit beta 2 | Visada | 1 ligoje |
| JAK3Janus kinase 3 | Visada | 2 ligose |
| MAN2B2mannosidase alpha class 2B member 2 | Visada | 1 ligoje |
| NDC1NDC1 transmembrane nucleoporin | Visada | 1 ligoje |
| NFKBIANFKB inhibitor alpha | Visada | 2 ligose |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Visada | 1 ligoje |
| PTCRApre T cell antigen receptor alpha | Visada | 1 ligoje |
| RELREL proto-oncogene, NF-kB subunit | Visada | 1 ligoje |
| SAMD9sterile alpha motif domain containing 9 | Visada | 1 ligoje |
| SKIC2SKI2 subunit of superkiller complex | Visada | 1 ligoje |
| SLC10A2solute carrier family 10 member 2 | Visada | 1 ligoje |
| SLC19A1solute carrier family 19 member 1 | Visada | 1 ligoje |
| SLC51Asolute carrier family 51 member A | Visada | 1 ligoje |
| SLC51BSLC51 subunit beta | Visada | 1 ligoje |
| SLC5A1solute carrier family 5 member 1 | Visada | 1 ligoje |
| STX3syntaxin 3 | Visada | 1 ligoje |
| TCF3transcription factor 3 | Visada | 1 ligoje |
| TOM1target of myb1 membrane trafficking protein | Visada | 1 ligoje |
| TRAF3TNF receptor associated factor 3 | Visada | 1 ligoje |
| VPS45vacuolar protein sorting 45 homolog | Visada | 1 ligoje |
| ZAP70zeta chain of T cell receptor associated protein kinase 70 | Visada | 2 ligose |
Rodyti dar 84 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| ANTXR2ANTXR cell adhesion molecule 2 | Labai dažnai (80–99%) | 1 ligoje |
| BTKBruton tyrosine kinase | Labai dažnai (80–99%) | 2 ligose |
| CHD7chromodomain helicase DNA binding protein 7 | Labai dažnai (80–99%) | 1 ligoje |
| EPCAMepithelial cell adhesion molecule | Labai dažnai (80–99%) | 1 ligoje |
| IL2RGinterleukin 2 receptor subunit gamma | Labai dažnai (80–99%) | 2 ligose |
| IL7Rinterleukin 7 receptor | Labai dažnai (80–99%) | 2 ligose |
| NBNnibrin | Labai dažnai (80–99%) | 1 ligoje |
| NUDCD3NudC domain containing 3 | Labai dažnai (80–99%) | 1 ligoje |
| PSMB10proteasome 20S subunit beta 10 | Labai dažnai (80–99%) | 1 ligoje |
| RAG1recombination activating 1 | Labai dažnai (80–99%) | 1 ligoje |
| RAG2recombination activating 2 | Labai dažnai (80–99%) | 1 ligoje |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Labai dažnai (80–99%) | 1 ligoje |
| SLC39A4solute carrier family 39 member 4 | Labai dažnai (80–99%) | 1 ligoje |
| WASWASP actin nucleation promoting factor | Labai dažnai (80–99%) | 2 ligose |
| AGR2anterior gradient 2, protein disulphide isomerase family member | Dažnai (30–79%) | 1 ligoje |
| ALG1ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Dažnai (30–79%) | 1 ligoje |
| ALKALK receptor tyrosine kinase | Dažnai (30–79%) | 1 ligoje |
| ATMATM serine/threonine kinase | Dažnai (30–79%) | 1 ligoje |
| ATP5F1AATP synthase F1 subunit alpha | Dažnai (30–79%) | 1 ligoje |
| ATP7AATPase copper transporting alpha | Dažnai (30–79%) | 1 ligoje |
| CASP8caspase 8 | Dažnai (30–79%) | 1 ligoje |
| CD3DCD3 delta subunit of T-cell receptor complex | Dažnai (30–79%) | 1 ligoje |
| COG6component of oligomeric golgi complex 6 | Dažnai (30–79%) | 1 ligoje |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Dažnai (30–79%) | 1 ligoje |
| ETHE1ETHE1 persulfide dioxygenase | Dažnai (30–79%) | 1 ligoje |
| FCHO1FCH and mu domain containing endocytic adaptor 1 | Dažnai (30–79%) | 1 ligoje |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Dažnai (30–79%) | 1 ligoje |
| IDUAalpha-L-iduronidase | Dažnai (30–79%) | 1 ligoje |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Dažnai (30–79%) | 1 ligoje |
| IL21Rinterleukin 21 receptor | Dažnai (30–79%) | 1 ligoje |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | Dažnai (30–79%) | 1 ligoje |
| IRF4interferon regulatory factor 4 | Dažnai (30–79%) | 1 ligoje |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | Dažnai (30–79%) | 1 ligoje |
| LMO1LIM domain only 1 | Dažnai (30–79%) | 1 ligoje |
| LRBALPS responsive beige-like anchor protein | Dažnai (30–79%) | 1 ligoje |
| MADDMAP kinase activating death domain | Dažnai (30–79%) | 2 ligose |
| MAP3K14mitogen-activated protein kinase kinase kinase 14 | Dažnai (30–79%) | 1 ligoje |
| MGME1mitochondrial genome maintenance exonuclease 1 | Dažnai (30–79%) | 1 ligoje |
| MTTPmicrosomal triglyceride transfer protein | Dažnai (30–79%) | 1 ligoje |
| MVKmevalonate kinase | Dažnai (30–79%) | 1 ligoje |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Dažnai (30–79%) | 1 ligoje |
| ORAI1ORAI calcium release-activated calcium modulator 1 | Dažnai (30–79%) | 1 ligoje |
| OTULINOTU deubiquitinase with linear linkage specificity | Dažnai (30–79%) | 1 ligoje |
| PHOX2Bpaired like homeobox 2B | Dažnai (30–79%) | 1 ligoje |
| POLA1DNA polymerase alpha 1, catalytic subunit | Dažnai (30–79%) | 1 ligoje |
| RBCK1RANBP2-type and C3HC4-type zinc finger containing 1 | Dažnai (30–79%) | 1 ligoje |
| RFXANKregulatory factor X associated ankyrin containing protein | Dažnai (30–79%) | 1 ligoje |
| RYR3ryanodine receptor 3 | Dažnai (30–79%) | 1 ligoje |
| SAA1serum amyloid A1 | Dažnai (30–79%) | 1 ligoje |
| SPINK5serine peptidase inhibitor Kazal type 5 | Dažnai (30–79%) | 2 ligose |
| TFRCtransferrin receptor | Dažnai (30–79%) | 1 ligoje |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Dažnai (30–79%) | 1 ligoje |
| VPS33BVPS33B late endosome and lysosome associated | Dažnai (30–79%) | 1 ligoje |
| ADNPactivity dependent neuroprotector homeobox | Kartais (5–29%) | 1 ligoje |
| CARD11caspase recruitment domain family member 11 | Kartais (5–29%) | 1 ligoje |
| CARMIL2capping protein regulator and myosin 1 linker 2 | Kartais (5–29%) | 1 ligoje |
| CCDC47coiled-coil domain containing 47 | Kartais (5–29%) | 1 ligoje |
| COG4component of oligomeric golgi complex 4 | Kartais (5–29%) | 1 ligoje |
| DOCK2dedicator of cytokinesis 2 | Kartais (5–29%) | 1 ligoje |
| GINS3GINS complex subunit 3 | Kartais (5–29%) | 1 ligoje |
| HEATR3HEAT repeat containing 3 | Kartais (5–29%) | 1 ligoje |
| IGHMimmunoglobulin heavy constant mu | Kartais (5–29%) | 1 ligoje |
| IPO8importin 8 | Kartais (5–29%) | 1 ligoje |
| ITCHitchy E3 ubiquitin protein ligase | Kartais (5–29%) | 1 ligoje |
| KMT5Blysine methyltransferase 5B | Kartais (5–29%) | 1 ligoje |
| PGM1phosphoglucomutase 1 | Kartais (5–29%) | 1 ligoje |
| PKP1plakophilin 1 | Kartais (5–29%) | 1 ligoje |
| PPP2R5Dprotein phosphatase 2 regulatory subunit B'delta | Kartais (5–29%) | 2 ligose |
| SLC35C1solute carrier family 35 member C1 | Kartais (5–29%) | 1 ligoje |
| SONSON DNA and RNA binding protein | Kartais (5–29%) | 2 ligose |
| SREBF1sterol regulatory element binding transcription factor 1 | Kartais (5–29%) | 1 ligoje |
| STAT5Bsignal transducer and activator of transcription 5B | Kartais (5–29%) | 1 ligoje |
| TNFRSF1ATNF receptor superfamily member 1A | Kartais (5–29%) | 1 ligoje |
| USP7ubiquitin specific peptidase 7 | Kartais (5–29%) | 1 ligoje |
| WDR83OSWD repeat domain 83 opposite strand | Kartais (5–29%) | 1 ligoje |
| ASAH1N-acylsphingosine amidohydrolase 1 | Retai (1–4 %) | 1 ligoje |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Retai (1–4 %) | 1 ligoje |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Neužfiksuota | 1 ligoje |
| FOXN1forkhead box N1 | Neužfiksuota | 1 ligoje |
| HEXBhexosaminidase subunit beta | Neužfiksuota | 1 ligoje |
| IKBKBinhibitor of nuclear factor kappa B kinase subunit beta | Neužfiksuota | 1 ligoje |
| RNF113Aring finger protein 113A | Neužfiksuota | 1 ligoje |
| TERTtelomerase reverse transcriptase | Neužfiksuota | 1 ligoje |
| TKFCtriokinase and FMN cyclase | Neužfiksuota | 1 ligoje |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
Platesni požymiai
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- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.19-9814e911.
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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 810+ physician-ready reports.
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