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PrisijungtiKlaustiSekvenuokite savo genomą↗
Požymis
Esodeviation
A manifest or latent ocular deviation in which one or both eyes tends to deviate nasally.
Santrauka
- Taip pat vadinama
- Convergent squint, Convergent strabismus
- Kūno sistema
- Abnormality of the eye
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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/esodeviation.json"
page <- fromJSON(url)
page$trait$nameEsodeviationHP:0020045
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Esodeviation, 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.
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout this report →
- Leukocyte Adhesion DeficiencyReads 1 of these genesSLC35C1About this report →
- Congenital Disorders of GlycosylationReads 5 of these genesALG12ALG2COG1PMM2SLC35C1About this report →
Show 28 more reports
- Familial Atrial FibrillationReads 1 of these genesGJA5About this report →
- Leigh SyndromeReads 4 of these genesDLATOPA1HPDLLRPPRCAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 1 of these genesCYB5R3About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Congenital Myasthenic SyndromeReads 2 of these genesSCN4AALG2About this report →
- VitreoretinopathyReads 2 of these genesNRLZNF408About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesITPR1About this report →
- Pyruvate Dehydrogenase & Pyruvate Carboxylase DeficiencyReads 1 of these genesDLATAbout this report →
- Intellectual DisabilityReads 5 of these genesKAT6ABPTFFBXO11PIDD1SATB2About this report →
- Meckel SyndromeReads 1 of these genesB9D1About this report →
- HyperinsulinismReads 1 of these genesPMM2About this report →
- Epilepsy (Full Panel)Reads 4 of these genesFLNAAARS1UFSP2PLPBPAbout this report →
- Hereditary Optic NeuropathyReads 1 of these genesOPA1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX12About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesPEX12AARS1About this report →
- Retinitis PigmentosaReads 2 of these genesNRLZNF408About this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesAHCYAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesKAT6AAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesCOL6A2About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesCOL6A2About this report →
- Primary Mitochondrial DiseaseReads 2 of these genesOPA1LRPPRCAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesITPR1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesSCN4AAbout this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesB9D1About this report →
- Dilated CardiomyopathyReads 1 of these genesABCC9About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesHPDLAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesAARS1About this report →
Vienu tyrimu sužinokite genus, susijusius su Esodeviation, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test49 genų susiję su Esodeviation
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Esodeviation. 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 |
|---|---|---|
| AHCYadenosylhomocysteinase | Visada | 1 ligoje |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Visada | 1 ligoje |
| ASNSasparagine synthetase (glutamine-hydrolyzing) | Visada | 1 ligoje |
| CYB5R3cytochrome b5 reductase 3 | Visada | 1 ligoje |
| FASTKD5FASTK mitochondrial RNA regulator 5 | Visada | 1 ligoje |
| FLNAfilamin A | Visada | 1 ligoje |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Visada | 1 ligoje |
| MED16mediator complex subunit 16 | Visada | 1 ligoje |
| NOTCH3notch receptor 3 | Visada | 1 ligoje |
| PEX12peroxisomal biogenesis factor 12 | Visada | 1 ligoje |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Visada | 1 ligoje |
| SCAF4SR-related CTD associated factor 4 | Visada | 1 ligoje |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Visada | 1 ligoje |
| KAT6Alysine acetyltransferase 6A | Labai dažnai (80–99%) | 1 ligoje |
| AARS1alanyl-tRNA synthetase 1 | Dažnai (30–79%) | 1 ligoje |
| ALG2ALG2 alpha-1,3/1,6-mannosyltransferase | Dažnai (30–79%) | 1 ligoje |
| B9D1B9 domain containing 1 | Dažnai (30–79%) | 1 ligoje |
| COG1component of oligomeric golgi complex 1 | Dažnai (30–79%) | 1 ligoje |
| COL6A2collagen type VI alpha 2 chain | Dažnai (30–79%) | 1 ligoje |
| DDX59DEAD-box helicase 59 | Dažnai (30–79%) | 1 ligoje |
| DLATdihydrolipoamide S-acetyltransferase | Dažnai (30–79%) | 1 ligoje |
| H4C3H4 clustered histone 3 | Dažnai (30–79%) | 1 ligoje |
| NRLneural retina leucine zipper | Dažnai (30–79%) | 1 ligoje |
| OPA1OPA1 mitochondrial dynamin like GTPase | Dažnai (30–79%) | 1 ligoje |
| PAK1p21 (RAC1) activated kinase 1 | Dažnai (30–79%) | 1 ligoje |
| PAN2poly(A) specific ribonuclease subunit PAN2 | Dažnai (30–79%) | 1 ligoje |
| PMM2phosphomannomutase 2 | Dažnai (30–79%) | 1 ligoje |
| PUS7pseudouridine synthase 7 | Dažnai (30–79%) | 1 ligoje |
| UFSP2UFM1 specific peptidase 2 | Dažnai (30–79%) | 1 ligoje |
| VPS50VPS50 subunit of EARP/GARPII complex | Dažnai (30–79%) | 1 ligoje |
| ZNF408zinc finger protein 408 | Dažnai (30–79%) | 1 ligoje |
| ABCC9ATP binding cassette subfamily C member 9 | Kartais (5–29%) | 1 ligoje |
| BPTFbromodomain PHD finger transcription factor | Kartais (5–29%) | 1 ligoje |
| CHMP1Acharged multivesicular body protein 1A | Kartais (5–29%) | 1 ligoje |
| DDB1damage specific DNA binding protein 1 | Kartais (5–29%) | 1 ligoje |
| FBXO11F-box protein 11 | Kartais (5–29%) | 1 ligoje |
| FOXP2forkhead box P2 | Kartais (5–29%) | 1 ligoje |
| HPDL4-hydroxyphenylpyruvate dioxygenase like | Kartais (5–29%) | 1 ligoje |
| KICS2KICSTOR subunit 2 | Kartais (5–29%) | 1 ligoje |
| LRPPRCleucine rich pentatricopeptide repeat containing | Kartais (5–29%) | 1 ligoje |
Rodyti dar 9 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| PI4KAphosphatidylinositol 4-kinase alpha | Kartais (5–29%) | 1 ligoje |
| PIDD1p53-induced death domain protein 1 | Kartais (5–29%) | 1 ligoje |
| PLPBPpyridoxal phosphate binding protein | Kartais (5–29%) | 1 ligoje |
| SATB2SATB homeobox 2 | Kartais (5–29%) | 1 ligoje |
| SLC35C1solute carrier family 35 member C1 | Kartais (5–29%) | 1 ligoje |
| TELO2telomere maintenance 2 | Kartais (5–29%) | 1 ligoje |
| TMEM222transmembrane protein 222 | Kartais (5–29%) | 1 ligoje |
| GJA5gap junction protein alpha 5 | Retai (1–4 %) | 1 ligoje |
| GJA8gap junction protein alpha 8 | Retai (1–4 %) | 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
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 2026.10.17-8666dff2.
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
From traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 470+ physician-ready reports.
Nuo 449 $
Nemokamas pristatymas · Rezultatai per 6–8 savaites
