AtlasTunnus
Colonic diverticula
The presence of multiple diverticula of the colon.
Kokkuvõte
- Teised nimetused
- Colonic diverticulosis
- Kehasüsteem
- Abnormality of the digestive system
AtlasSelle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/colonic-diverticula.json"
page <- fromJSON(url)
page$trait$nameLugege välja geenid, mis on seotud Colonic diverticula-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test27 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.
- Johanson-Blizzard SyndromeReads 1 of these genesUBR1About this report →
- Lynch SyndromeReads 2 of these genesMLH1MSH2About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
Show 23 more reports
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesRETAbout this report →
- Cutis LaxaReads 2 of these genesEFEMP1ELNAbout this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Ehlers-Danlos SyndromeReads 2 of these genesCHST14DSEAbout this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesERBB3About this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT3About this report →
- GlaucomaReads 1 of these genesEFEMP1About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesRETAbout this report →
- Hereditary Macular DystrophiesReads 1 of these genesEFEMP1About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesRETAbout this report →
- DNA Repair DiseaseReads 2 of these genesMLH1MSH2About this report →
- Polycystic Kidney DiseaseReads 1 of these genesPKD1About this report →
- Urinary and Renal System TumourReads 1 of these genesRETAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Primary Mitochondrial DiseaseReads 3 of these genesDNAJC30POLGTYMPAbout this report →
- Autoimmune DiseaseReads 1 of these genesSTAT3About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesCHST14DSEAbout this report →
- Thyroid CancerReads 1 of these genesRETAbout this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Other Inborn Errors of ImmunityReads 2 of these genesNCF1STAT3About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesPOLGTYMPAbout this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesPOLGAbout this report →
Lugege välja geenid, mis on seotud Colonic diverticula-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test33 geeni on seotud tunnusega Colonic diverticula
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Colonic diverticula. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| EFEMP1EGF-like fibulin extracellular matrix protein 1 | Alati | Esineb 1 haiguses |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Sageli (30–79%) | Esineb 1 haiguses |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Sageli (30–79%) | Esineb 1 haiguses |
| CHST14carbohydrate sulfotransferase 14 | Sageli (30–79%) | Esineb 1 haiguses |
| CLIP2CAP-Gly domain containing linker protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Sageli (30–79%) | Esineb 1 haiguses |
| DSEdermatan sulfate epimerase | Sageli (30–79%) | Esineb 1 haiguses |
| EIF4Heukaryotic translation initiation factor 4H | Sageli (30–79%) | Esineb 1 haiguses |
| ELNelastin | Sageli (30–79%) | Esineb 2 haiguses |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Sageli (30–79%) | Esineb 1 haiguses |
| GTF2Igeneral transcription factor IIi | Sageli (30–79%) | Esineb 1 haiguses |
| GTF2IRD1GTF2I repeat domain containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GTF2IRD2GTF2I repeat domain containing 2 | Sageli (30–79%) | Esineb 1 haiguses |
| LIMK1LIM domain kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| METTL27methyltransferase like 27 | Sageli (30–79%) | Esineb 1 haiguses |
| MLXIPLMLX interacting protein like | Sageli (30–79%) | Esineb 1 haiguses |
| NCF1neutrophil cytosolic factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Sageli (30–79%) | Esineb 1 haiguses |
| RFC2replication factor C subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| STX1Asyntaxin 1A | Sageli (30–79%) | Esineb 1 haiguses |
| TBL2transducin beta like 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TMEM270transmembrane protein 270 | Sageli (30–79%) | Esineb 1 haiguses |
| TYMPthymidine phosphorylase | Sageli (30–79%) | Esineb 1 haiguses |
| VPS37DVPS37D subunit of ESCRT-I | Sageli (30–79%) | Esineb 1 haiguses |
| STAT3signal transducer and activator of transcription 3 | Harva (1–4%) | Esineb 1 haiguses |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Pole registreeritud | Esineb 1 haiguses |
| MLH1mutL homolog 1 | Pole registreeritud | Esineb 1 haiguses |
| MSH2mutS homolog 2 | Pole registreeritud | Esineb 1 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Pole registreeritud | Esineb 1 haiguses |
| PKD1polycystin 1, transient receptor potential channel interacting | Pole registreeritud | Esineb 1 haiguses |
| PTENphosphatase and tensin homolog | Pole registreeritud | Esineb 1 haiguses |
| RETret proto-oncogene | Pole registreeritud | Esineb 1 haiguses |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.19-9814e911.
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Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
