Požymis
Abnormal circulating lipid concentration
Any deviation from the normal concentration of lipid in the blood circulation.
Santrauka
- Taip pat vadinama
- Abnormal lipid level
- Kūno sistema
- Laboratory abnormality
Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/abnormal-circulating-lipid-concentration.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Abnormal circulating lipid concentration, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test31 condition report reads 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.
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
- Androgen Insensitivity SyndromeReads 1 of these genesARAbout this report →
- Fabry DiseaseReads 1 of these genesGLAAbout this report →
- Spinal and Bulbar Muscular Atrophy (Kennedy Disease)Reads 1 of these genesARAbout this report →
Show 27 more reports
- Hereditary HypolipoproteinemiasReads 2 of these genesABCA1APOA1About this report →
- CitrullinemiaReads 1 of these genesSLC25A13About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Marfan Like SyndromesReads 1 of these genesFBN1About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 1 of these genesIL12RB1About this report →
- HyperinsulinismReads 1 of these genesABCC8About this report →
- Hereditary AmyloidosisReads 1 of these genesAPOA1About this report →
- LipodystrophyReads 1 of these genesLIPEAbout this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesABCC8About this report →
- Urea Cycle DisorderReads 1 of these genesSLC25A13About this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Lysosomal Storage DiseaseReads 2 of these genesGLASMPD1About this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 1 of these genesHRAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesARAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesABCC8About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesLAMB1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesTBCKAbout this report →
- Diabetes MellitusReads 1 of these genesABCC8About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesTNPO3About this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesAPOA1SMPD1About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesTBCKARAbout this report →
- Primary Mitochondrial DiseaseReads 1 of these genesDNAJC30About this report →
- Epilepsy (Full Panel)Reads 1 of these genesLMNB2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesNCF1About this report →
Vienu tyrimu sužinokite genus, susijusius su Abnormal circulating lipid concentration, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test40 genų susiję su Abnormal circulating lipid concentration
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Abnormal circulating lipid concentration. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| ABCC8ATP binding cassette subfamily C member 8 | Visada | 1 ligoje |
| LAMB1laminin subunit beta 1 | Visada | 1 ligoje |
| ABCA1ATP binding cassette subfamily A member 1 | Labai dažnai (80–99%) | 1 ligoje |
| APOA1apolipoprotein A1 | Labai dažnai (80–99%) | 1 ligoje |
| SLC25A13solute carrier family 25 member 13 | Labai dažnai (80–99%) | 1 ligoje |
| GLAgalactosidase alpha | Dažnai (30–79%) | 1 ligoje |
| IL12Ainterleukin 12A | Dažnai (30–79%) | 1 ligoje |
| IL12RB1interleukin 12 receptor subunit beta 1 | Dažnai (30–79%) | 1 ligoje |
| IRF5interferon regulatory factor 5 | Dažnai (30–79%) | 1 ligoje |
| MMEL1membrane metalloendopeptidase like 1 | Dažnai (30–79%) | 1 ligoje |
| POU2AF1POU class 2 homeobox associating factor 1 | Dažnai (30–79%) | 1 ligoje |
| SMPD1sphingomyelin phosphodiesterase 1 | Dažnai (30–79%) | 1 ligoje |
| SPIBSpi-B transcription factor | Dažnai (30–79%) | 1 ligoje |
| TBCKTBC1 domain containing kinase | Dažnai (30–79%) | 1 ligoje |
| TNFSF15TNF superfamily member 15 | Dažnai (30–79%) | 1 ligoje |
| TNPO3transportin 3 | Dažnai (30–79%) | 1 ligoje |
| ARandrogen receptor | Kartais (5–29%) | 1 ligoje |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Kartais (5–29%) | 1 ligoje |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Kartais (5–29%) | 1 ligoje |
| CLIP2CAP-Gly domain containing linker protein 2 | Kartais (5–29%) | 1 ligoje |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Kartais (5–29%) | 1 ligoje |
| EIF4Heukaryotic translation initiation factor 4H | Kartais (5–29%) | 1 ligoje |
| ELNelastin | Kartais (5–29%) | 1 ligoje |
| FBN1fibrillin 1 | Kartais (5–29%) | 1 ligoje |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Kartais (5–29%) | 1 ligoje |
| GTF2Igeneral transcription factor IIi | Kartais (5–29%) | 1 ligoje |
| GTF2IRD1GTF2I repeat domain containing 1 | Kartais (5–29%) | 1 ligoje |
| GTF2IRD2GTF2I repeat domain containing 2 | Kartais (5–29%) | 1 ligoje |
| HRHR lysine demethylase and nuclear receptor corepressor | Kartais (5–29%) | 1 ligoje |
| LIMK1LIM domain kinase 1 | Kartais (5–29%) | 1 ligoje |
| METTL27methyltransferase like 27 | Kartais (5–29%) | 1 ligoje |
| NCF1neutrophil cytosolic factor 1 | Kartais (5–29%) | 1 ligoje |
| RFC2replication factor C subunit 2 | Kartais (5–29%) | 1 ligoje |
| STX1Asyntaxin 1A | Kartais (5–29%) | 1 ligoje |
| TBL2transducin beta like 2 | Kartais (5–29%) | 1 ligoje |
| TMEM270transmembrane protein 270 | Kartais (5–29%) | 1 ligoje |
| VPS37DVPS37D subunit of ESCRT-I | Kartais (5–29%) | 1 ligoje |
| LIPElipase E, hormone sensitive type | Neužfiksuota | 1 ligoje |
| LMNB2lamin B2 | Neužfiksuota | 1 ligoje |
| XRCC4X-ray repair cross complementing 4 | Neužfiksuota | 1 ligoje |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
Siauresni požymiai
- Elevated lipids in blood45 genų
- Abnormality of cholesterol metabolism6 genų
- Abnormal circulating fatty acid concentration2 genų
- Elevated circulating C-triol concentration2 genų
- Elevated circulating sitosterol concentration2 genų
- Elevated circulating dimethyl sterol concentration1 genas
- Elevated circulating lysosphingomyelin concentration1 genas
- Elevated circulating methysterol concentration1 genas
- Elevated circulating monomethyl sterol concentration1 genas
- Hyperapobetalipoproteinemia1 genas
- Increased circulating farnesol concentration1 genas
- Abnormal circulating beta-carotene concentration
- Abnormal circulating phospholipid concentration
- Hypolipidemia
Platesni požymiai
Iš kur tai žinoma
- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.19-9814e911.
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