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Merkmal
Chronic diarrhea
The presence of chronic diarrhea, which is usually taken to mean diarrhea that has persisted for over 4 weeks.
Zusammenfassung
- Auch genannt
- Diarrhea, recurrent, Recurrent diarrhea, Chronic diarrhoea
- Körpersystem
- Abnormality of the digestive system
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Diese Seite als Daten
Hängen Sie .json an die Adresse der Seite an oder fordern Sie application/json an, um sie als JSON zu lesen.
library(jsonlite)
url <- "https://dantelabs.com/traits/chronic-diarrhea.json"
page <- fromJSON(url)
page$trait$nameChronic diarrheaHP:0002028
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Meinen Genome Test bestellen80 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.
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- IPEX Syndrome and Other TregopathiesReads 4 of these genesBACH2FOXP3IL2RALRBAAbout this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 2 of these genesPIK3CDPIK3R1About this report →
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- 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 →
- 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 →
Lesen Sie die Gene aus, die mit Chronic diarrhea zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
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Meinen Genome Test bestellen124 Gene mit Chronic diarrhea verknüpft
Veränderungen in diesen Genen verursachen seltene Erkrankungen, bei denen Chronic diarrhea auftritt. Die meisten Menschen mit diesem Merkmal haben keine dieser Erkrankungen, und ein Gen auf dieser Liste sagt nichts über das eigene Genom einer Person aus.
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| ADAadenosine deaminase | Immer | In 2 Erkrankungen |
| ATP6AP1ATPase H+ transporting accessory protein 1 | Immer | In 1 Erkrankung |
| B2Mbeta-2-microglobulin | Immer | In 1 Erkrankung |
| BACH2BACH transcriptional regulator 2 | Immer | In 1 Erkrankung |
| CARD8caspase recruitment domain family member 8 | Immer | In 1 Erkrankung |
| CD3GCD3 gamma subunit of T-cell receptor complex | Immer | In 1 Erkrankung |
| CHASERRCHD2 adjacent suppressive regulatory RNA | Immer | In 1 Erkrankung |
| CLMPCXADR like cell adhesion molecule | Immer | In 1 Erkrankung |
| CR2complement C3d receptor 2 | Immer | In 1 Erkrankung |
| DCLRE1CDNA cross-link repair 1C | Immer | In 2 Erkrankungen |
| DNASE2deoxyribonuclease 2, lysosomal | Immer | In 1 Erkrankung |
| FLT3LGfms related receptor tyrosine kinase 3 ligand | Immer | In 1 Erkrankung |
| FOXP3forkhead box P3 | Immer | In 1 Erkrankung |
| GUCY2Cguanylate cyclase 2C | Immer | In 2 Erkrankungen |
| HYOU1hypoxia up-regulated 1 | Immer | In 1 Erkrankung |
| IGKCimmunoglobulin kappa constant | Immer | In 1 Erkrankung |
| IKZF2IKAROS family zinc finger 2 | Immer | In 1 Erkrankung |
| IL2RAinterleukin 2 receptor subunit alpha | Immer | In 1 Erkrankung |
| IL6STinterleukin 6 cytokine family signal transducer | Immer | In 1 Erkrankung |
| ITGB2integrin subunit beta 2 | Immer | In 1 Erkrankung |
| JAK3Janus kinase 3 | Immer | In 2 Erkrankungen |
| MAN2B2mannosidase alpha class 2B member 2 | Immer | In 1 Erkrankung |
| NDC1NDC1 transmembrane nucleoporin | Immer | In 1 Erkrankung |
| NFKBIANFKB inhibitor alpha | Immer | In 2 Erkrankungen |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Immer | In 1 Erkrankung |
| PTCRApre T cell antigen receptor alpha | Immer | In 1 Erkrankung |
| RELREL proto-oncogene, NF-kB subunit | Immer | In 1 Erkrankung |
| SAMD9sterile alpha motif domain containing 9 | Immer | In 1 Erkrankung |
| SKIC2SKI2 subunit of superkiller complex | Immer | In 1 Erkrankung |
| SLC10A2solute carrier family 10 member 2 | Immer | In 1 Erkrankung |
| SLC19A1solute carrier family 19 member 1 | Immer | In 1 Erkrankung |
| SLC51Asolute carrier family 51 member A | Immer | In 1 Erkrankung |
| SLC51BSLC51 subunit beta | Immer | In 1 Erkrankung |
| SLC5A1solute carrier family 5 member 1 | Immer | In 1 Erkrankung |
| STX3syntaxin 3 | Immer | In 1 Erkrankung |
| TCF3transcription factor 3 | Immer | In 1 Erkrankung |
| TOM1target of myb1 membrane trafficking protein | Immer | In 1 Erkrankung |
| TRAF3TNF receptor associated factor 3 | Immer | In 1 Erkrankung |
| VPS45vacuolar protein sorting 45 homolog | Immer | In 1 Erkrankung |
| ZAP70zeta chain of T cell receptor associated protein kinase 70 | Immer | In 2 Erkrankungen |
84 weitere Gene anzeigen
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| ANTXR2ANTXR cell adhesion molecule 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| BTKBruton tyrosine kinase | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| CHD7chromodomain helicase DNA binding protein 7 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| EPCAMepithelial cell adhesion molecule | Sehr häufig (80–99 %) | In 1 Erkrankung |
| IL2RGinterleukin 2 receptor subunit gamma | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| IL7Rinterleukin 7 receptor | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| NBNnibrin | Sehr häufig (80–99 %) | In 1 Erkrankung |
| NUDCD3NudC domain containing 3 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PSMB10proteasome 20S subunit beta 10 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| RAG1recombination activating 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| RAG2recombination activating 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SLC39A4solute carrier family 39 member 4 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| WASWASP actin nucleation promoting factor | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| AGR2anterior gradient 2, protein disulphide isomerase family member | Häufig (30–79 %) | In 1 Erkrankung |
| ALG1ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Häufig (30–79 %) | In 1 Erkrankung |
| ALKALK receptor tyrosine kinase | Häufig (30–79 %) | In 1 Erkrankung |
| ATMATM serine/threonine kinase | Häufig (30–79 %) | In 1 Erkrankung |
| ATP5F1AATP synthase F1 subunit alpha | Häufig (30–79 %) | In 1 Erkrankung |
| ATP7AATPase copper transporting alpha | Häufig (30–79 %) | In 1 Erkrankung |
| CASP8caspase 8 | Häufig (30–79 %) | In 1 Erkrankung |
| CD3DCD3 delta subunit of T-cell receptor complex | Häufig (30–79 %) | In 1 Erkrankung |
| COG6component of oligomeric golgi complex 6 | Häufig (30–79 %) | In 1 Erkrankung |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Häufig (30–79 %) | In 1 Erkrankung |
| ETHE1ETHE1 persulfide dioxygenase | Häufig (30–79 %) | In 1 Erkrankung |
| FCHO1FCH and mu domain containing endocytic adaptor 1 | Häufig (30–79 %) | In 1 Erkrankung |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Häufig (30–79 %) | In 1 Erkrankung |
| IDUAalpha-L-iduronidase | Häufig (30–79 %) | In 1 Erkrankung |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Häufig (30–79 %) | In 1 Erkrankung |
| IL21Rinterleukin 21 receptor | Häufig (30–79 %) | In 1 Erkrankung |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | Häufig (30–79 %) | In 1 Erkrankung |
| IRF4interferon regulatory factor 4 | Häufig (30–79 %) | In 1 Erkrankung |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | Häufig (30–79 %) | In 1 Erkrankung |
| LMO1LIM domain only 1 | Häufig (30–79 %) | In 1 Erkrankung |
| LRBALPS responsive beige-like anchor protein | Häufig (30–79 %) | In 1 Erkrankung |
| MADDMAP kinase activating death domain | Häufig (30–79 %) | In 2 Erkrankungen |
| MAP3K14mitogen-activated protein kinase kinase kinase 14 | Häufig (30–79 %) | In 1 Erkrankung |
| MGME1mitochondrial genome maintenance exonuclease 1 | Häufig (30–79 %) | In 1 Erkrankung |
| MTTPmicrosomal triglyceride transfer protein | Häufig (30–79 %) | In 1 Erkrankung |
| MVKmevalonate kinase | Häufig (30–79 %) | In 1 Erkrankung |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Häufig (30–79 %) | In 1 Erkrankung |
| ORAI1ORAI calcium release-activated calcium modulator 1 | Häufig (30–79 %) | In 1 Erkrankung |
| OTULINOTU deubiquitinase with linear linkage specificity | Häufig (30–79 %) | In 1 Erkrankung |
| PHOX2Bpaired like homeobox 2B | Häufig (30–79 %) | In 1 Erkrankung |
| POLA1DNA polymerase alpha 1, catalytic subunit | Häufig (30–79 %) | In 1 Erkrankung |
| RBCK1RANBP2-type and C3HC4-type zinc finger containing 1 | Häufig (30–79 %) | In 1 Erkrankung |
| RFXANKregulatory factor X associated ankyrin containing protein | Häufig (30–79 %) | In 1 Erkrankung |
| RYR3ryanodine receptor 3 | Häufig (30–79 %) | In 1 Erkrankung |
| SAA1serum amyloid A1 | Häufig (30–79 %) | In 1 Erkrankung |
| SPINK5serine peptidase inhibitor Kazal type 5 | Häufig (30–79 %) | In 2 Erkrankungen |
| TFRCtransferrin receptor | Häufig (30–79 %) | In 1 Erkrankung |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Häufig (30–79 %) | In 1 Erkrankung |
| VPS33BVPS33B late endosome and lysosome associated | Häufig (30–79 %) | In 1 Erkrankung |
| ADNPactivity dependent neuroprotector homeobox | Manchmal (5–29 %) | In 1 Erkrankung |
| CARD11caspase recruitment domain family member 11 | Manchmal (5–29 %) | In 1 Erkrankung |
| CARMIL2capping protein regulator and myosin 1 linker 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| CCDC47coiled-coil domain containing 47 | Manchmal (5–29 %) | In 1 Erkrankung |
| COG4component of oligomeric golgi complex 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| DOCK2dedicator of cytokinesis 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| GINS3GINS complex subunit 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| HEATR3HEAT repeat containing 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| IGHMimmunoglobulin heavy constant mu | Manchmal (5–29 %) | In 1 Erkrankung |
| IPO8importin 8 | Manchmal (5–29 %) | In 1 Erkrankung |
| ITCHitchy E3 ubiquitin protein ligase | Manchmal (5–29 %) | In 1 Erkrankung |
| KMT5Blysine methyltransferase 5B | Manchmal (5–29 %) | In 1 Erkrankung |
| PGM1phosphoglucomutase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| PKP1plakophilin 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| PPP2R5Dprotein phosphatase 2 regulatory subunit B'delta | Manchmal (5–29 %) | In 2 Erkrankungen |
| SLC35C1solute carrier family 35 member C1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SONSON DNA and RNA binding protein | Manchmal (5–29 %) | In 2 Erkrankungen |
| SREBF1sterol regulatory element binding transcription factor 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| STAT5Bsignal transducer and activator of transcription 5B | Manchmal (5–29 %) | In 1 Erkrankung |
| TNFRSF1ATNF receptor superfamily member 1A | Manchmal (5–29 %) | In 1 Erkrankung |
| USP7ubiquitin specific peptidase 7 | Manchmal (5–29 %) | In 1 Erkrankung |
| WDR83OSWD repeat domain 83 opposite strand | Manchmal (5–29 %) | In 1 Erkrankung |
| ASAH1N-acylsphingosine amidohydrolase 1 | Selten (1–4 %) | In 1 Erkrankung |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Selten (1–4 %) | In 1 Erkrankung |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Nicht erfasst | In 1 Erkrankung |
| FOXN1forkhead box N1 | Nicht erfasst | In 1 Erkrankung |
| HEXBhexosaminidase subunit beta | Nicht erfasst | In 1 Erkrankung |
| IKBKBinhibitor of nuclear factor kappa B kinase subunit beta | Nicht erfasst | In 1 Erkrankung |
| RNF113Aring finger protein 113A | Nicht erfasst | In 1 Erkrankung |
| TERTtelomerase reverse transcriptase | Nicht erfasst | In 1 Erkrankung |
| TKFCtriokinase and FMN cyclase | Nicht erfasst | In 1 Erkrankung |
Wie häufig dieses Merkmal bei Menschen mit einer der Erkrankungen auftritt, die mit dem Gen in Verbindung stehen, und zwar der höchste Wert unter ihnen, so wie ihn die Human Phenotype Ontology erfasst. Diese Seiten beschreiben Merkmale und die dazugehörige Forschung; sie stellen keine Diagnose dar. Fragen zu Symptomen richten Sie bitte an Ihre Ärztin, Ihren Arzt oder eine genetische Beratung.
Übergeordnete Merkmale
Woher diese Angaben stammen
- Die Human Phenotype Ontology, Version 2026-09-01: das Merkmal, seine Bezeichnungen, seine Definition und die damit verknüpften Gene. Weitere Informationen finden Sie unter hpo.jax.org.
- Datenstand 2026.10.19-9814e911.
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