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Požymis
Abnormality of the eyebrow
Klinikinis pavadinimas: Abnormal eyebrow morphology
An abnormality of the eyebrow.
Santrauka
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PrisijungtiKlaustiSekvenuokite savo genomą↗
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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-eyebrow-morphology.json"
page <- fromJSON(url)
page$trait$nameAbnormality of the eyebrowHP:0000534
AtlasKam mes padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Abnormality of the eyebrow, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo 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.
- Dyskeratosis CongenitaReads 12 of these genesACDCTC1DKC1NHP2NOP10NPM1About this report →
- Waardenburg SyndromeReads 4 of these genesEDN3EDNRBMITFSOX10About this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 6 of these genesDSG4KRT81KRT83KRT86CDSNKRT74About this report →
- Familial Pulmonary FibrosisReads 3 of these genesPARNRTEL1TERTAbout this report →
Show 28 more reports
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- H SyndromeReads 1 of these genesSLC29A3About this report →
- Radio-Tartaglia SyndromeReads 1 of these genesSPENAbout this report →
- Roberts SyndromeReads 1 of these genesESCO2About this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 2 of these genesTERCTERTAbout this report →
- Acrodermatitis EnteropathicaReads 1 of these genesSLC39A4About this report →
- Marfan Like SyndromesReads 2 of these genesFBN1SKIAbout this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 2 of these genesPEX1PEX6About this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 1 of these genesREREAbout this report →
- MelanomaReads 1 of these genesMITFAbout this report →
- VitreoretinopathyReads 2 of these genesXYLT2CTC1About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesFASAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Dilated CardiomyopathyReads 2 of these genesLMNAPRDM16About this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesPEX1PEX6About this report →
- Autoimmune DiseaseReads 1 of these genesFASAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesSKIAbout this report →
- Inherited IchthyosesReads 1 of these genesCDSNAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesPEX1PEX6LMNAAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesXYLT2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesPEX6About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesPEX1PEX6About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesFASAbout this report →
Vienu tyrimu sužinokite genus, susijusius su Abnormality of the eyebrow, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test52 genų susiję su Abnormality of the eyebrow
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Abnormality of the eyebrow. 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 |
|---|---|---|
| DSG4desmoglein 4 | Labai dažnai (80–99%) | 1 ligoje |
| EDN3endothelin 3 | Labai dažnai (80–99%) | 1 ligoje |
| EDNRBendothelin receptor type B | Labai dažnai (80–99%) | 1 ligoje |
| FASFas cell surface death receptor | Labai dažnai (80–99%) | 1 ligoje |
| FBN1fibrillin 1 | Labai dažnai (80–99%) | 1 ligoje |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Labai dažnai (80–99%) | 1 ligoje |
| KRT81keratin 81 | Labai dažnai (80–99%) | 1 ligoje |
| KRT83keratin 83 | Labai dažnai (80–99%) | 1 ligoje |
| KRT86keratin 86 | Labai dažnai (80–99%) | 1 ligoje |
| LTBP3latent transforming growth factor beta binding protein 3 | Labai dažnai (80–99%) | 1 ligoje |
| MITFmelanocyte inducing transcription factor | Labai dažnai (80–99%) | 1 ligoje |
| PEX1peroxisomal biogenesis factor 1 | Labai dažnai (80–99%) | 1 ligoje |
| PEX6peroxisomal biogenesis factor 6 | Labai dažnai (80–99%) | 1 ligoje |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Labai dažnai (80–99%) | 1 ligoje |
| SLC39A4solute carrier family 39 member 4 | Labai dažnai (80–99%) | 1 ligoje |
| SMOC1SPARC related modular calcium binding 1 | Labai dažnai (80–99%) | 1 ligoje |
| SOX10SRY-box transcription factor 10 | Labai dažnai (80–99%) | 2 ligose |
| XYLT2xylosyltransferase 2 | Labai dažnai (80–99%) | 1 ligoje |
| CASZ1castor zinc finger 1 | Dažnai (30–79%) | 1 ligoje |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Dažnai (30–79%) | 1 ligoje |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Dažnai (30–79%) | 1 ligoje |
| HSPG2heparan sulfate proteoglycan 2 | Dažnai (30–79%) | 2 ligose |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Dažnai (30–79%) | 1 ligoje |
| LMNAlamin A/C | Dažnai (30–79%) | 1 ligoje |
| LUZP1leucine zipper protein 1 | Dažnai (30–79%) | 1 ligoje |
| MMP23Bmatrix metallopeptidase 23B | Dažnai (30–79%) | 1 ligoje |
| PDPNpodoplanin | Dažnai (30–79%) | 1 ligoje |
| PRDM16PR/SET domain 16 | Dažnai (30–79%) | 1 ligoje |
| PRKCZprotein kinase C zeta | Dažnai (30–79%) | 1 ligoje |
| REREarginine-glutamic acid dipeptide repeats | Dažnai (30–79%) | 1 ligoje |
| SKISKI proto-oncogene | Dažnai (30–79%) | 1 ligoje |
| SPENspen family transcriptional repressor | Dažnai (30–79%) | 1 ligoje |
| UBE4Bubiquitination factor E4B | Dažnai (30–79%) | 1 ligoje |
| ACDACD shelterin complex subunit and telomerase recruitment factor | Kartais (5–29%) | 1 ligoje |
| CTC1CST telomere replication complex component 1 | Kartais (5–29%) | 1 ligoje |
| DKC1dyskerin pseudouridine synthase 1 | Kartais (5–29%) | 1 ligoje |
| NHP2NHP2 ribonucleoprotein | Kartais (5–29%) | 1 ligoje |
| NOP10NOP10 ribonucleoprotein | Kartais (5–29%) | 1 ligoje |
| NPM1nucleophosmin 1 | Kartais (5–29%) | 1 ligoje |
| PARNpoly(A)-specific ribonuclease | Kartais (5–29%) | 1 ligoje |
Rodyti dar 12 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| RTEL1regulator of telomere elongation helicase 1 | Kartais (5–29%) | 1 ligoje |
| SLC29A3solute carrier family 29 member 3 | Kartais (5–29%) | 1 ligoje |
| TERCtelomerase RNA component | Kartais (5–29%) | 1 ligoje |
| TERTtelomerase reverse transcriptase | Kartais (5–29%) | 1 ligoje |
| TINF2TERF1 interacting nuclear factor 2 | Kartais (5–29%) | 1 ligoje |
| TYMSthymidylate synthetase | Kartais (5–29%) | 1 ligoje |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Kartais (5–29%) | 1 ligoje |
| WRAP53WD repeat containing antisense to TP53 | Kartais (5–29%) | 1 ligoje |
| ZNF699zinc finger protein 699 | Kartais (5–29%) | 1 ligoje |
| CDSNcorneodesmosin | Neužfiksuota | 1 ligoje |
| KRT74keratin 74 | Neužfiksuota | 1 ligoje |
| SCARF2scavenger receptor class F member 2 | 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
- Highly arched eyebrow225 genų
- Monobrow219 genų
- Thick eyebrow170 genų
- Sparse or absent eyebrows55 genų
- Medial flaring of the eyebrow40 genų
- Horizontal eyebrow36 genų
- Broad eyebrow29 genų
- White eyebrow11 genų
- Laterally extended eyebrow5 genų
- Long eyebrows5 genų
- Abnormal location of the eyebrow1 genas
- Double eyebrow1 genas
- Drooping brow1 genas
- Laterally curved eyebrow1 genas
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.
AtlasKam mes padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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