Atlas이런 분들을 위해과학적 근거제품연구 성과
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형질
Chronic diarrhea
The presence of chronic diarrhea, which is usually taken to mean diarrhea that has persisted for over 4 weeks.
요약
- 다른 명칭
- Diarrhea, recurrent, Recurrent diarrhea, Chronic diarrhoea
Atlas이런 분들을 위해과학적 근거제품연구 성과
로그인질문하기유전체를 시퀀싱하세요↗
이 페이지의 데이터
페이지 주소 끝에 .json을 붙이거나 application/json을 요청하면 JSON 형식으로 읽을 수 있습니다.
library(jsonlite)
url <- "https://dantelabs.com/traits/chronic-diarrhea.json"
page <- fromJSON(url)
page$trait$nameChronic diarrheaHP:0002028
Atlas이런 분들을 위해과학적 근거제품연구 성과
로그인질문하기유전체를 시퀀싱하세요↗
81 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.
- 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 →
연관 유전자 124개: Chronic diarrhea
이 유전자들의 변화는 Chronic diarrhea 증상이 나타나는 희귀 질환을 일으킵니다. 이 형질을 가진 대부분의 사람에게는 이러한 질환이 없으며, 이 목록에 있는 유전자가 누구의 개인 유전체에 대해서도 말해 주는 것은 없습니다.
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| ADAadenosine deaminase | 항상 | 질환 2개에서 나타남 |
| ATP6AP1ATPase H+ transporting accessory protein 1 | 항상 | 질환 1개에서 나타남 |
| B2Mbeta-2-microglobulin | 항상 | 질환 1개에서 나타남 |
| BACH2BACH transcriptional regulator 2 | 항상 | 질환 1개에서 나타남 |
| CARD8caspase recruitment domain family member 8 | 항상 | 질환 1개에서 나타남 |
| CD3GCD3 gamma subunit of T-cell receptor complex | 항상 | 질환 1개에서 나타남 |
| CHASERRCHD2 adjacent suppressive regulatory RNA | 항상 | 질환 1개에서 나타남 |
| CLMPCXADR like cell adhesion molecule | 항상 | 질환 1개에서 나타남 |
| CR2complement C3d receptor 2 | 항상 | 질환 1개에서 나타남 |
| DCLRE1CDNA cross-link repair 1C | 항상 | 질환 2개에서 나타남 |
| DNASE2deoxyribonuclease 2, lysosomal | 항상 | 질환 1개에서 나타남 |
| FLT3LGfms related receptor tyrosine kinase 3 ligand | 항상 | 질환 1개에서 나타남 |
| FOXP3forkhead box P3 | 항상 | 질환 1개에서 나타남 |
| GUCY2Cguanylate cyclase 2C | 항상 | 질환 2개에서 나타남 |
| HYOU1hypoxia up-regulated 1 | 항상 | 질환 1개에서 나타남 |
| IGKCimmunoglobulin kappa constant | 항상 | 질환 1개에서 나타남 |
| IKZF2IKAROS family zinc finger 2 | 항상 | 질환 1개에서 나타남 |
| IL2RAinterleukin 2 receptor subunit alpha | 항상 | 질환 1개에서 나타남 |
| IL6STinterleukin 6 cytokine family signal transducer | 항상 | 질환 1개에서 나타남 |
| ITGB2integrin subunit beta 2 | 항상 | 질환 1개에서 나타남 |
| JAK3Janus kinase 3 | 항상 | 질환 2개에서 나타남 |
| MAN2B2mannosidase alpha class 2B member 2 | 항상 | 질환 1개에서 나타남 |
| NDC1NDC1 transmembrane nucleoporin | 항상 | 질환 1개에서 나타남 |
| NFKBIANFKB inhibitor alpha | 항상 | 질환 2개에서 나타남 |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | 항상 | 질환 1개에서 나타남 |
| PTCRApre T cell antigen receptor alpha | 항상 | 질환 1개에서 나타남 |
| RELREL proto-oncogene, NF-kB subunit | 항상 | 질환 1개에서 나타남 |
| SAMD9sterile alpha motif domain containing 9 | 항상 | 질환 1개에서 나타남 |
| SKIC2SKI2 subunit of superkiller complex | 항상 | 질환 1개에서 나타남 |
| SLC10A2solute carrier family 10 member 2 | 항상 | 질환 1개에서 나타남 |
| SLC19A1solute carrier family 19 member 1 | 항상 | 질환 1개에서 나타남 |
| SLC51Asolute carrier family 51 member A | 항상 | 질환 1개에서 나타남 |
| SLC51BSLC51 subunit beta | 항상 | 질환 1개에서 나타남 |
| SLC5A1solute carrier family 5 member 1 | 항상 | 질환 1개에서 나타남 |
| STX3syntaxin 3 | 항상 | 질환 1개에서 나타남 |
| TCF3transcription factor 3 | 항상 | 질환 1개에서 나타남 |
| TOM1target of myb1 membrane trafficking protein | 항상 | 질환 1개에서 나타남 |
| TRAF3TNF receptor associated factor 3 | 항상 | 질환 1개에서 나타남 |
| VPS45vacuolar protein sorting 45 homolog | 항상 | 질환 1개에서 나타남 |
| ZAP70zeta chain of T cell receptor associated protein kinase 70 | 항상 | 질환 2개에서 나타남 |
유전자 84개 더 보기
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| ANTXR2ANTXR cell adhesion molecule 2 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| BTKBruton tyrosine kinase | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| CHD7chromodomain helicase DNA binding protein 7 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| EPCAMepithelial cell adhesion molecule | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| IL2RGinterleukin 2 receptor subunit gamma | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| IL7Rinterleukin 7 receptor | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| NBNnibrin | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| NUDCD3NudC domain containing 3 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| PSMB10proteasome 20S subunit beta 10 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| RAG1recombination activating 1 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| RAG2recombination activating 2 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| SLC39A4solute carrier family 39 member 4 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| WASWASP actin nucleation promoting factor | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| AGR2anterior gradient 2, protein disulphide isomerase family member | 자주 (30–79%) | 질환 1개에서 나타남 |
| ALG1ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | 자주 (30–79%) | 질환 1개에서 나타남 |
| ALKALK receptor tyrosine kinase | 자주 (30–79%) | 질환 1개에서 나타남 |
| ATMATM serine/threonine kinase | 자주 (30–79%) | 질환 1개에서 나타남 |
| ATP5F1AATP synthase F1 subunit alpha | 자주 (30–79%) | 질환 1개에서 나타남 |
| ATP7AATPase copper transporting alpha | 자주 (30–79%) | 질환 1개에서 나타남 |
| CASP8caspase 8 | 자주 (30–79%) | 질환 1개에서 나타남 |
| CD3DCD3 delta subunit of T-cell receptor complex | 자주 (30–79%) | 질환 1개에서 나타남 |
| COG6component of oligomeric golgi complex 6 | 자주 (30–79%) | 질환 1개에서 나타남 |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| ETHE1ETHE1 persulfide dioxygenase | 자주 (30–79%) | 질환 1개에서 나타남 |
| FCHO1FCH and mu domain containing endocytic adaptor 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| IDUAalpha-L-iduronidase | 자주 (30–79%) | 질환 1개에서 나타남 |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | 자주 (30–79%) | 질환 1개에서 나타남 |
| IL21Rinterleukin 21 receptor | 자주 (30–79%) | 질환 1개에서 나타남 |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| IRF4interferon regulatory factor 4 | 자주 (30–79%) | 질환 1개에서 나타남 |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | 자주 (30–79%) | 질환 1개에서 나타남 |
| LMO1LIM domain only 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| LRBALPS responsive beige-like anchor protein | 자주 (30–79%) | 질환 1개에서 나타남 |
| MADDMAP kinase activating death domain | 자주 (30–79%) | 질환 2개에서 나타남 |
| MAP3K14mitogen-activated protein kinase kinase kinase 14 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MGME1mitochondrial genome maintenance exonuclease 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MTTPmicrosomal triglyceride transfer protein | 자주 (30–79%) | 질환 1개에서 나타남 |
| MVKmevalonate kinase | 자주 (30–79%) | 질환 1개에서 나타남 |
| MYCNMYCN proto-oncogene, bHLH transcription factor | 자주 (30–79%) | 질환 1개에서 나타남 |
| ORAI1ORAI calcium release-activated calcium modulator 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| OTULINOTU deubiquitinase with linear linkage specificity | 자주 (30–79%) | 질환 1개에서 나타남 |
| PHOX2Bpaired like homeobox 2B | 자주 (30–79%) | 질환 1개에서 나타남 |
| POLA1DNA polymerase alpha 1, catalytic subunit | 자주 (30–79%) | 질환 1개에서 나타남 |
| RBCK1RANBP2-type and C3HC4-type zinc finger containing 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| RFXANKregulatory factor X associated ankyrin containing protein | 자주 (30–79%) | 질환 1개에서 나타남 |
| RYR3ryanodine receptor 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SAA1serum amyloid A1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SPINK5serine peptidase inhibitor Kazal type 5 | 자주 (30–79%) | 질환 2개에서 나타남 |
| TFRCtransferrin receptor | 자주 (30–79%) | 질환 1개에서 나타남 |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | 자주 (30–79%) | 질환 1개에서 나타남 |
| VPS33BVPS33B late endosome and lysosome associated | 자주 (30–79%) | 질환 1개에서 나타남 |
| ADNPactivity dependent neuroprotector homeobox | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CARD11caspase recruitment domain family member 11 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CARMIL2capping protein regulator and myosin 1 linker 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CCDC47coiled-coil domain containing 47 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| COG4component of oligomeric golgi complex 4 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| DOCK2dedicator of cytokinesis 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| GINS3GINS complex subunit 3 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| HEATR3HEAT repeat containing 3 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IGHMimmunoglobulin heavy constant mu | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IPO8importin 8 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ITCHitchy E3 ubiquitin protein ligase | 가끔 (5–29%) | 질환 1개에서 나타남 |
| KMT5Blysine methyltransferase 5B | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PGM1phosphoglucomutase 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PKP1plakophilin 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PPP2R5Dprotein phosphatase 2 regulatory subunit B'delta | 가끔 (5–29%) | 질환 2개에서 나타남 |
| SLC35C1solute carrier family 35 member C1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SONSON DNA and RNA binding protein | 가끔 (5–29%) | 질환 2개에서 나타남 |
| SREBF1sterol regulatory element binding transcription factor 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| STAT5Bsignal transducer and activator of transcription 5B | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TNFRSF1ATNF receptor superfamily member 1A | 가끔 (5–29%) | 질환 1개에서 나타남 |
| USP7ubiquitin specific peptidase 7 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| WDR83OSWD repeat domain 83 opposite strand | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ASAH1N-acylsphingosine amidohydrolase 1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | 기록되지 않음 | 질환 1개에서 나타남 |
| FOXN1forkhead box N1 | 기록되지 않음 | 질환 1개에서 나타남 |
| HEXBhexosaminidase subunit beta | 기록되지 않음 | 질환 1개에서 나타남 |
| IKBKBinhibitor of nuclear factor kappa B kinase subunit beta | 기록되지 않음 | 질환 1개에서 나타남 |
| RNF113Aring finger protein 113A | 기록되지 않음 | 질환 1개에서 나타남 |
| TERTtelomerase reverse transcriptase | 기록되지 않음 | 질환 1개에서 나타남 |
| TKFCtriokinase and FMN cyclase | 기록되지 않음 | 질환 1개에서 나타남 |
Human Phenotype Ontology가 기록한, 해당 유전자와 관련된 질환을 가진 사람들 가운데 이 특징이 나타나는 빈도입니다. 이 페이지는 특징과 그 바탕이 되는 연구를 설명하며, 진단이 아닙니다. 증상에 대해서는 의사나 유전 상담사에게 문의하시기 바랍니다.
상위 형질
출처
- Human Phenotype Ontology, 버전 2026-09-01: 특징, 명칭, 정의 및 이와 연결된 유전자입니다. 자세한 내용은 hpo.jax.org에서 확인하실 수 있습니다.
- 데이터 버전 2026.10.19-9814e911.
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