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Træk
Weakness of muscles controlling eye movement
Klinisk navn: Ophthalmoparesis
Ophthalmoplegia is a paralysis or weakness of one or more of the muscles that control eye movement.
Resumé
- Også kaldet
- Extraocular muscle palsy, Extraocular muscle paralysis, Weakness of extraocular eye movement
- Kropssystem
- Abnormality of the eye
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Denne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/ophthalmoparesis.json"
page <- fromJSON(url)
page$trait$nameHvem vi hjælperVores videnskabProdukterResultater
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Læs de gener, der er knyttet til Weakness of muscles controlling eye movement, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test36 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.
- Congenital Myasthenic SyndromeReads 11 of these genesCHRNEGFPT1MUSKSLC5A7PLECCOL13A1About this report →
- Primary Mitochondrial DiseaseReads 21 of these genesAFG3L2COX10COX15COX6B1FASTKD2POLGAbout this report →
- Leigh SyndromeReads 12 of these genesCOX10SCO2SURF1TACO1MT-ATP6MT-ND1About this report →
- Malignant Hyperthermia SusceptibilityReads 2 of these genesRYR1CACNA1SAbout this report →
Show 32 more reports
- Hereditary Optic NeuropathyReads 5 of these genesAFG3L2MT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Congenital MyopathiesReads 6 of these genesDNM2BIN1KLHL40RYR1SPEGTTNAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 20 of these genesCOX10POLGSCO2SLC5A7SURF1TACO1About this report →
- Familial Periodic ParalysisReads 2 of these genesSCN4ACACNA1SAbout this report →
- Hyperprolinaemia Type 2Reads 1 of these genesALDH4A1About this report →
- PLEC-Related Epidermolysis Bullosa and Muscular DystrophyReads 1 of these genesPLECAbout this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 5 of these genesAFG3L2ATN1ATXN7ATXN1ATXN2About this report →
- Inherited Neurodegenerative DisordersReads 16 of these genesAFG3L2POLGSLC5A7TUBA4AATN1ATXN7About this report →
- Syndromic and Metabolic CardiomyopathiesReads 2 of these genesSLC25A4ACTN2About this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A4About this report →
- Distal MyopathiesReads 3 of these genesGIPC1LRP12TTNAbout this report →
- Charcot-Marie-Tooth DiseaseReads 5 of these genesSCO2SLC5A7SURF1DNM2MPV17About this report →
- Myofibrillar MyopathiesReads 2 of these genesRYR1TTNAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesPLECTTNAbout this report →
- Hereditary AmyloidosisReads 1 of these genesGSNAbout this report →
- Dilated CardiomyopathyReads 2 of these genesSYNE1TTNAbout this report →
- Frontotemporal DementiaReads 1 of these genesMAPTAbout this report →
- Female InfertilityReads 2 of these genesTUBA4ATWNKAbout this report →
- OsteopetrosisReads 1 of these genesTCIRG1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesTWNKSYNE1About this report →
- Parkinson DiseaseReads 1 of these genesMAPTAbout this report →
- Epidermolysis BullosaReads 1 of these genesPLECAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesGSNAbout this report →
- Spinal Muscular AtrophyReads 1 of these genesSLC5A7About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesTUBA4AAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesDOK7About this report →
- Nephrotic SyndromeReads 1 of these genesLAMB2About this report →
- Diabetes MellitusReads 1 of these genesMT-TL1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesSCN4AAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesUCHL1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesGABRA3About this report →
Læs de gener, der er knyttet til Weakness of muscles controlling eye movement, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test80 gener knyttet til Weakness of muscles controlling eye movement
Ændringer i disse gener forårsager sjældne tilstande, hvor Weakness of muscles controlling eye movement ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| AFG3L2AFG3 like matrix AAA peptidase subunit 2 | Altid | I 3 tilstande |
| CHRNEcholinergic receptor nicotinic epsilon subunit | Altid | I 2 tilstande |
| COX10cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 | Altid | I 1 tilstand |
| COX15cytochrome c oxidase assembly factor COX15 | Altid | I 1 tilstand |
| COX6B1cytochrome c oxidase subunit 6B1 | Altid | I 1 tilstand |
| FASTKD2FASTK mitochondrial RNA regulator 2 | Altid | I 1 tilstand |
| GFPT1glutamine--fructose-6-phosphate transaminase 1 | Altid | I 2 tilstande |
| ISCUiron-sulfur cluster assembly enzyme | Altid | I 1 tilstand |
| JPH1junctophilin 1 | Altid | I 1 tilstand |
| MT-TNmitochondrially encoded tRNA-Asn (AAU/C) | Altid | I 1 tilstand |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Altid | I 1 tilstand |
| MUSKmuscle associated receptor tyrosine kinase | Altid | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Altid | I 6 tilstande |
| SCO1synthesis of cytochrome C oxidase 1 | Altid | I 1 tilstand |
| SCO2synthesis of cytochrome C oxidase 2 | Altid | I 1 tilstand |
| SLC5A7solute carrier family 5 member 7 | Altid | I 1 tilstand |
| SURF1SURF1 cytochrome c oxidase assembly factor | Altid | I 1 tilstand |
| TACO1translational activator of cytochrome c oxidase I | Altid | I 1 tilstand |
| TEFMtranscription elongation factor, mitochondrial | Altid | I 1 tilstand |
| TUBA4Atubulin alpha 4a | Altid | I 1 tilstand |
| TYMPthymidine phosphorylase | Altid | I 2 tilstande |
| ABCD3ATP binding cassette subfamily D member 3 | Meget ofte (80–99 %) | I 1 tilstand |
| GIPC1GIPC PDZ domain containing family member 1 | Meget ofte (80–99 %) | I 1 tilstand |
| LRP12LDL receptor related protein 12 | Meget ofte (80–99 %) | I 2 tilstande |
| NOTCH2NLCnotch 2 N-terminal like C | Meget ofte (80–99 %) | I 1 tilstand |
| NUTM2B-AS1NUTM2B antisense RNA 1 | Meget ofte (80–99 %) | I 1 tilstand |
| PLECplectin | Meget ofte (80–99 %) | I 1 tilstand |
| RILPL1Rab interacting lysosomal protein like 1 | Meget ofte (80–99 %) | I 1 tilstand |
| ATN1atrophin 1 | Ofte (30–79 %) | I 1 tilstand |
| ATXN7ataxin 7 | Ofte (30–79 %) | I 1 tilstand |
| COL13A1collagen type XIII alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| COLQcollagen like tail subunit of asymmetric acetylcholinesterase | Ofte (30–79 %) | I 2 tilstande |
| DNM2dynamin 2 | Ofte (30–79 %) | I 1 tilstand |
| GUK1guanylate kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| HLA-Bmajor histocompatibility complex, class I, B | Ofte (30–79 %) | I 1 tilstand |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Ofte (30–79 %) | I 1 tilstand |
| LAMB2laminin subunit beta 2 | Ofte (30–79 %) | I 1 tilstand |
| LIG3DNA ligase 3 | Ofte (30–79 %) | I 1 tilstand |
| MPV17mitochondrial inner membrane protein MPV17 | Ofte (30–79 %) | I 1 tilstand |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Ofte (30–79 %) | I 1 tilstand |
Vis 40 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| MT-ND3mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 | Ofte (30–79 %) | I 1 tilstand |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Ofte (30–79 %) | I 1 tilstand |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Ofte (30–79 %) | I 1 tilstand |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Ofte (30–79 %) | I 1 tilstand |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Ofte (30–79 %) | I 2 tilstande |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Ofte (30–79 %) | I 1 tilstand |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Ofte (30–79 %) | I 1 tilstand |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Ofte (30–79 %) | I 1 tilstand |
| MTMR14myotubularin related protein 14 | Ofte (30–79 %) | I 1 tilstand |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Ofte (30–79 %) | I 1 tilstand |
| POLG2DNA polymerase gamma 2, accessory subunit | Ofte (30–79 %) | I 1 tilstand |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Ofte (30–79 %) | I 1 tilstand |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Ofte (30–79 %) | I 2 tilstande |
| SLC25A4solute carrier family 25 member 4 | Ofte (30–79 %) | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Ofte (30–79 %) | I 3 tilstande |
| UCHL1ubiquitin C-terminal hydrolase L1 | Ofte (30–79 %) | I 1 tilstand |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Nogle gange (5–29 %) | I 1 tilstand |
| ATXN1ataxin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ATXN2ataxin 2 | Nogle gange (5–29 %) | I 1 tilstand |
| BIN1bridging integrator 1 | Nogle gange (5–29 %) | I 1 tilstand |
| DNA2DNA replication helicase/nuclease 2 | Nogle gange (5–29 %) | I 1 tilstand |
| DOK7docking protein 7 | Nogle gange (5–29 %) | I 1 tilstand |
| GSNgelsolin | Nogle gange (5–29 %) | I 1 tilstand |
| KLHL40kelch like family member 40 | Nogle gange (5–29 %) | I 1 tilstand |
| RNASEH1ribonuclease H1 | Nogle gange (5–29 %) | I 1 tilstand |
| RYR1ryanodine receptor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Nogle gange (5–29 %) | I 3 tilstande |
| SPEGstriated muscle enriched protein kinase | Nogle gange (5–29 %) | I 1 tilstand |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TTNtitin | Nogle gange (5–29 %) | I 1 tilstand |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Sjældent (1–4%) | I 1 tilstand |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | Sjældent (1–4%) | I 1 tilstand |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Sjældent (1–4%) | I 1 tilstand |
| ACTN2actinin alpha 2 | Ikke registreret | I 1 tilstand |
| CHATcholine O-acetyltransferase | Ikke registreret | I 1 tilstand |
| CHRNA1cholinergic receptor nicotinic alpha 1 subunit | Ikke registreret | I 2 tilstande |
| MAPTmicrotubule associated protein tau | Ikke registreret | I 1 tilstand |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
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Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
AtlasHvem vi hjælperVores videnskabProdukterResultater
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Read the genes behind these traits in your own DNA.
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