AtlasTratto
Intermittent diarrhea
Repeated episodes of diarrhea separated by periods without diarrhea.
Riepilogo
- Detto anche
- Episodic diarrhea, Episodic diarrhoea, Intermittent diarrhoea
- Sistema corporeo
- Abnormality of the digestive system
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library(jsonlite)
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page$trait$nameLeggi i geni collegati a Intermittent diarrhea e il resto del tuo genoma con un unico test.
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Ottieni il mio 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 →
Leggi i geni collegati a Intermittent diarrhea e il resto del tuo genoma con un unico test.
A partire da 449 $Spedizione gratuita · Risultati in 6–8 settimane
Ottieni il mio Genome Test27 geni collegati a Intermittent diarrhea
Alterazioni in questi geni causano malattie rare in cui si osserva Intermittent diarrhea. La maggior parte delle persone con questo tratto non presenta nessuna di tali condizioni, e un gene di questo elenco non dice nulla sul genoma di nessuno in particolare.
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| FLT3LGfms related receptor tyrosine kinase 3 ligand | Sempre | In 1 condizione |
| NHEJ1non-homologous end joining factor 1 | Sempre | In 1 condizione |
| RNF31ring finger protein 31 | Sempre | In 1 condizione |
| ATP6V0A1ATPase H+ transporting V0 subunit a1 | Spesso (30–79%) | In 1 condizione |
| ATRXATRX chromatin remodeler | Spesso (30–79%) | In 1 condizione |
| COG4component of oligomeric golgi complex 4 | Spesso (30–79%) | In 1 condizione |
| ETFAelectron transfer flavoprotein subunit alpha | Spesso (30–79%) | In 1 condizione |
| ETFBelectron transfer flavoprotein subunit beta | Spesso (30–79%) | In 1 condizione |
| ETFDHelectron transfer flavoprotein dehydrogenase | Spesso (30–79%) | In 1 condizione |
| GATA6GATA binding protein 6 | Spesso (30–79%) | In 1 condizione |
| TLK2tousled like kinase 2 | Spesso (30–79%) | In 1 condizione |
| UBE3Cubiquitin protein ligase E3C | Spesso (30–79%) | In 1 condizione |
| ACSF3acyl-CoA synthetase family member 3 | A volte (5–29%) | In 1 condizione |
| BRCA1BRCA1 DNA repair associated | A volte (5–29%) | In 1 condizione |
| BRCA2BRCA2 DNA repair associated | A volte (5–29%) | In 1 condizione |
| CDKN2Acyclin dependent kinase inhibitor 2A | A volte (5–29%) | In 1 condizione |
| DOCK2dedicator of cytokinesis 2 | A volte (5–29%) | In 1 condizione |
| KRASKRas proto-oncogene, GTPase | A volte (5–29%) | In 1 condizione |
| PALB2partner and localizer of BRCA2 | A volte (5–29%) | In 1 condizione |
| PALLDpalladin, cytoskeletal associated protein | A volte (5–29%) | In 1 condizione |
| RABL3RAB, member of RAS oncogene family like 3 | A volte (5–29%) | In 1 condizione |
| SMAD4SMAD family member 4 | A volte (5–29%) | In 1 condizione |
| TP53tumor protein p53 | A volte (5–29%) | In 1 condizione |
| ZNFX1zinc finger NFX1-type containing 1 | A volte (5–29%) | In 1 condizione |
| G6PC1glucose-6-phosphatase catalytic subunit 1 | Non registrato | In 1 condizione |
| POLGDNA polymerase gamma, catalytic subunit | Non registrato | In 1 condizione |
| TYMPthymidine phosphorylase | Non registrato | In 1 condizione |
Con quale frequenza questo tratto si presenta tra le persone con una delle condizioni legate al gene, nella misura più alta riscontrata tra queste, secondo quanto registrato dall'Human Phenotype Ontology. Queste pagine descrivono tratti e la ricerca che li riguarda; non costituiscono una diagnosi, e per i sintomi il medico o il consulente genetico è la persona a cui rivolgersi.
Tratti più generali
Fonte dei dati
- Human Phenotype Ontology, versione 2026-09-01: il tratto, i suoi nomi, la sua definizione e i geni a esso collegati. Per saperne di più visiti hpo.jax.org.
- Versione dei dati 2026.10.19-9814e911.
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