AtlasTræk
Intermittent diarrhea
Repeated episodes of diarrhea separated by periods without diarrhea.
Resumé
- Også kaldet
- Episodic diarrhea, Episodic diarrhoea, Intermittent diarrhoea
- Kropssystem
- Abnormality of the digestive system
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Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/intermittent-diarrhea.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Intermittent diarrhea, og resten af dit genom, med én test.
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Bestil min Genome Test32 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.
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- Saul-Wilson SyndromeReads 1 of these genesCOG4About this report →
Show 28 more reports
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 3 of these genesETFAETFBETFDHAbout this report →
- Fanconi AnemiaReads 3 of these genesBRCA1BRCA2PALB2About this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Hypertrophic CardiomyopathyReads 4 of these genesETFAETFBETFDHKRASAbout this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- MelanomaReads 1 of these genesCDKN2AAbout this report →
- DNA Repair DiseaseReads 3 of these genesBRCA1BRCA2PALB2About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Malignant Endocrine NeoplasmReads 1 of these genesTP53About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 1 of these genesPALB2About this report →
- Kidney CancerReads 1 of these genesTP53About this report →
- Urinary and Renal System TumourReads 1 of these genesTP53About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesGATA6About this report →
- Other Inborn Errors of ImmunityReads 4 of these genesNHEJ1DOCK2KRASZNFX1About this report →
- Methylmalonic & Propionic AcidemiaReads 1 of these genesACSF3About this report →
- Glycogen Storage DiseaseReads 1 of these genesG6PC1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesGATA6About this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Noonan SyndromeReads 1 of these genesKRASAbout this report →
- Intellectual DisabilityReads 3 of these genesATRXTLK2SMAD4About this report →
- Diabetes MellitusReads 1 of these genesGATA6About this report →
- Severe Combined ImmunodeficiencyReads 1 of these genesNHEJ1About this report →
- Primary Mitochondrial DiseaseReads 2 of these genesPOLGTYMPAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesPOLGTYMPAbout this report →
- Congenital Disorders of GlycosylationReads 1 of these genesCOG4About this report →
- Epilepsy (Full Panel)Reads 1 of these genesATP6V0A1About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesPOLGAbout this report →
Læs de gener, der er knyttet til Intermittent diarrhea, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test27 gener knyttet til Intermittent diarrhea
Ændringer i disse gener forårsager sjældne tilstande, hvor Intermittent diarrhea ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| FLT3LGfms related receptor tyrosine kinase 3 ligand | Altid | I 1 tilstand |
| NHEJ1non-homologous end joining factor 1 | Altid | I 1 tilstand |
| RNF31ring finger protein 31 | Altid | I 1 tilstand |
| ATP6V0A1ATPase H+ transporting V0 subunit a1 | Ofte (30–79 %) | I 1 tilstand |
| ATRXATRX chromatin remodeler | Ofte (30–79 %) | I 1 tilstand |
| COG4component of oligomeric golgi complex 4 | Ofte (30–79 %) | I 1 tilstand |
| ETFAelectron transfer flavoprotein subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| ETFBelectron transfer flavoprotein subunit beta | Ofte (30–79 %) | I 1 tilstand |
| ETFDHelectron transfer flavoprotein dehydrogenase | Ofte (30–79 %) | I 1 tilstand |
| GATA6GATA binding protein 6 | Ofte (30–79 %) | I 1 tilstand |
| TLK2tousled like kinase 2 | Ofte (30–79 %) | I 1 tilstand |
| UBE3Cubiquitin protein ligase E3C | Ofte (30–79 %) | I 1 tilstand |
| ACSF3acyl-CoA synthetase family member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| BRCA1BRCA1 DNA repair associated | Nogle gange (5–29 %) | I 1 tilstand |
| BRCA2BRCA2 DNA repair associated | Nogle gange (5–29 %) | I 1 tilstand |
| CDKN2Acyclin dependent kinase inhibitor 2A | Nogle gange (5–29 %) | I 1 tilstand |
| DOCK2dedicator of cytokinesis 2 | Nogle gange (5–29 %) | I 1 tilstand |
| KRASKRas proto-oncogene, GTPase | Nogle gange (5–29 %) | I 1 tilstand |
| PALB2partner and localizer of BRCA2 | Nogle gange (5–29 %) | I 1 tilstand |
| PALLDpalladin, cytoskeletal associated protein | Nogle gange (5–29 %) | I 1 tilstand |
| RABL3RAB, member of RAS oncogene family like 3 | Nogle gange (5–29 %) | I 1 tilstand |
| SMAD4SMAD family member 4 | Nogle gange (5–29 %) | I 1 tilstand |
| TP53tumor protein p53 | Nogle gange (5–29 %) | I 1 tilstand |
| ZNFX1zinc finger NFX1-type containing 1 | Nogle gange (5–29 %) | I 1 tilstand |
| G6PC1glucose-6-phosphatase catalytic subunit 1 | Ikke registreret | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Ikke registreret | I 1 tilstand |
| TYMPthymidine phosphorylase | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
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