AtlasTunnus
Low blood sugar when fasting
Kliiniline nimetus: Fasting hypoglycemia
Kokkuvõte
- Kehasüsteem
- Laboratory abnormality
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Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/fasting-hypoglycemia.json"
page <- fromJSON(url)
page$trait$nameLugege välja geenid, mis on seotud Low blood sugar when fasting-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test19 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.
- Glycogen Storage DiseaseReads 6 of these genesG6PC1SLC2A2PHKA2PHKBPHKG2GYS2About this report →
- Severe Inherited Insulin ResistanceReads 2 of these genesINSRAKT2About this report →
- Maturity-Onset Diabetes Of The YoungReads 4 of these genesABCC8HNF4AKCNJ11HNF1AAbout this report →
- Hereditary Fructose Intolerance & Gluconeogenesis DefectsReads 2 of these genesFBP1PCK1About this report →
Show 15 more reports
- Diabetes MellitusReads 6 of these genesSLC2A2ABCC8HNF4AKCNJ11AKT2HNF1AAbout this report →
- HyperinsulinismReads 3 of these genesABCC8INSRKCNJ11About this report →
- Neonatal Diabetes MellitusReads 3 of these genesSLC2A2ABCC8KCNJ11About this report →
- Thyroid Hormone Resistance, Transport & Metabolism DefectsReads 1 of these genesSECISBP2About this report →
- Fanconi Renotubular Syndrome and Renal GlucosuriaReads 1 of these genesHNF4AAbout this report →
- Classic Organic AciduriasReads 1 of these genesGCDHAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesIGF2About this report →
- LipodystrophyReads 1 of these genesAKT2About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesSLC25A20About this report →
- Congenital HypothyroidismReads 1 of these genesSECISBP2About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesTBX19About this report →
- Thyroid CancerReads 1 of these genesSECISBP2About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesTBX19About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesIGF2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesIARS2About this report →
Lugege välja geenid, mis on seotud Low blood sugar when fasting-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test22 geeni on seotud tunnusega Low blood sugar when fasting
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Low blood sugar when fasting. 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 |
|---|---|---|
| G6PC1glucose-6-phosphatase catalytic subunit 1 | Alati | Esineb 1 haiguses |
| SLC2A2solute carrier family 2 member 2 | Alati | Esineb 2 haiguses |
| ABCC8ATP binding cassette subfamily C member 8 | Väga sageli (80–99%) | Esineb 1 haiguses |
| HNF4Ahepatocyte nuclear factor 4 alpha | Väga sageli (80–99%) | Esineb 1 haiguses |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Väga sageli (80–99%) | Esineb 1 haiguses |
| INSRinsulin receptor | Väga sageli (80–99%) | Esineb 4 haiguses |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC25A20solute carrier family 25 member 20 | Väga sageli (80–99%) | Esineb 1 haiguses |
| AKT2AKT serine/threonine kinase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| FBP1fructose-bisphosphatase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GRB10growth factor receptor bound protein 10 | Sageli (30–79%) | Esineb 1 haiguses |
| HNF1AHNF1 homeobox A | Sageli (30–79%) | Esineb 1 haiguses |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PHKBphosphorylase kinase regulatory subunit beta | Sageli (30–79%) | Esineb 1 haiguses |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Sageli (30–79%) | Esineb 2 haiguses |
| GCDHglutaryl-CoA dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| SECISBP2SECIS binding protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GYS2glycogen synthase 2 | Pole registreeritud | Esineb 1 haiguses |
| IGF2insulin like growth factor 2 | Pole registreeritud | Esineb 1 haiguses |
| PCK1phosphoenolpyruvate carboxykinase 1 | Pole registreeritud | Esineb 1 haiguses |
| SLC1A1solute carrier family 1 member 1 | Pole registreeritud | Esineb 1 haiguses |
| TBX19T-box transcription factor 19 | 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
