AtlasDla kogo jest Dante LabsNasza naukaProduktyWyniki
Zaloguj sięZapytajZsekwencjonuj swój genom↗
Cecha
Abnormal full-field electroretinogram
An anomaly observed by full-field electroretinogram (ffERG). The ffERG measures the light-induced electrical activity of the retina at the corneal surface. Specifically, the ffERG records the global or total retinal electrical response to a full-field (Ganzfield) light stimulus. Isolation of the rod and cone components has important diagnostic value in differentiating between various retinal diseases. Modifying the properties of the light-stimulus (wavelength, strength, and flicker rate) as well as the adaptive state of the retina can separate the rod and cone functions of the ffERG.
Podsumowanie
- Układ organizmu
- Abnormality of the eye
AtlasDla kogo jest Dante LabsNasza naukaProduktyWyniki
Zaloguj sięZapytajZsekwencjonuj swój genom↗
Share this page
Ta strona jako dane
Aby odczytać ją jako JSON, dodaj .json na końcu adresu strony lub zażądaj application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/abnormal-full-field-electroretinogram.json"
page <- fromJSON(url)
page$trait$nameAbnormal full-field electroretinogramHP:0030466
AtlasDla kogo jest Dante LabsNasza naukaProduktyWyniki
Zaloguj sięZapytajZsekwencjonuj swój genom↗
Odczytaj geny powiązane z Abnormal full-field electroretinogram oraz resztę swojego genomu za pomocą jednego badania.
Od 449 $Bezpłatna wysyłka · Wyniki w ciągu 6–8 tygodni
Zamawiam Genome Test56 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.
- Retinitis PigmentosaReads 75 of these genesABCA4AGBL5AHRARHGEF18ARL2BPARL3About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 20 of these genesAIPL1CEP290CRB1CRXGUCY2DIMPDH1About this report →
- Congenital Stationary Night BlindnessReads 8 of these genesCABP4CACNA1FGUCY2DPDE6BPRPH2RHOAbout this report →
- Bardet-Biedl and Alström SyndromesReads 8 of these genesALMS1ARL6BBS1BBS2CEP290CFAP418About this report →
Show 52 more reports
- Hereditary Macular DystrophiesReads 5 of these genesBEST1PRPH2RLBP1ROM1RP1L1About this report →
- AchromatopsiaReads 4 of these genesATF6CNGA3OPN1LWOPN1MWAbout this report →
- VitreoretinopathyReads 6 of these genesBEST1KCNJ13NR2E3NRLVCANZNF408About this report →
- Colour Vision DeficiencyReads 2 of these genesOPN1LWOPN1MWAbout this report →
- RDH5-Related Retinopathy (Fundus Albipunctatus)Reads 2 of these genesPRPH2RLBP1About this report →
- Stargardt DiseaseReads 2 of these genesABCA4PROM1About this report →
- ADAM9-Related Cone-Rod DystrophyReads 1 of these genesADAM9About this report →
- CACNA2D4-Related RetinopathyReads 1 of these genesCACNA2D4About this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Cone-Rod Dystrophy 20 (POC1B)Reads 1 of these genesPOC1BAbout this report →
- GUCY2D-Related Dominant Cone-Rod DystrophyReads 1 of these genesGUCY2DAbout this report →
- GUCY2D-Related Recessive RetinopathyReads 1 of these genesGUCY2DAbout this report →
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
- IMPG1-Related Dominant RetinopathyReads 1 of these genesIMPG1About this report →
- IMPG1-Related RetinopathyReads 1 of these genesIMPG1About this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- PROM1-Related Recessive RetinopathyReads 1 of these genesPROM1About this report →
- RAB28-Related Cone-Rod DystrophyReads 1 of these genesRAB28About this report →
- RDH12-Related Early-Onset Retinal DystrophyReads 1 of these genesRDH12About this report →
- Spondylometaphyseal Dysplasia With Cone-Rod DystrophyReads 1 of these genesPCYT1AAbout this report →
- TTLL5-Related RetinopathyReads 1 of these genesTTLL5About this report →
- TUBB4B-Related CiliopathyReads 1 of these genesTUBB4BAbout this report →
- Joubert Syndrome And Related DisordersReads 6 of these genesAHI1ARL3CC2D2ACEP290OFD1TMEM216About this report →
- Age-Related Macular DegenerationReads 1 of these genesMFSD8About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 2 of these genesFOXC1PAX6About this report →
- Usher SyndromeReads 2 of these genesCLRN1USH2AAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 4 of these genesAHI1CC2D2ACEP290TMEM216About this report →
- Mucopolysaccharidosis Type III (Sanfilippo Syndrome)Reads 1 of these genesHGSNATAbout this report →
- Multiple Synostoses Syndrome (FGF9)Reads 1 of these genesGDF6About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesIFT43About this report →
- GlaucomaReads 1 of these genesFOXC1About this report →
- Autism Spectrum DisorderReads 1 of these genesRIMS1About this report →
- Kidney CancerReads 1 of these genesPAX6About this report →
- Polycystic Kidney DiseaseReads 1 of these genesIFT140About this report →
- Urinary and Renal System TumourReads 1 of these genesPAX6About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesMFSD8About this report →
- Lysosomal Storage DiseaseReads 2 of these genesHGSNATMFSD8About this report →
- Inherited Neurodegenerative DisordersReads 5 of these genesAHI1CC2D2ACEP290MFSD8TMEM216About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesIQCB1About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesKLHL7About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesRNU4-2About this report →
- Syndromic CraniosynostosisReads 1 of these genesIFT43About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesDHDDSPOMGNT1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesOTX2About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesOTX2About this report →
- Congenital Muscular DystrophiesReads 1 of these genesPOMGNT1About this report →
- Nephrotic SyndromeReads 1 of these genesCOQ8BAbout this report →
- Diabetes MellitusReads 1 of these genesPAX6About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesPOMGNT1About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesOTX2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesKLHL7About this report →
- Intellectual DisabilityReads 1 of these genesSCAPERAbout this report →
Odczytaj geny powiązane z Abnormal full-field electroretinogram oraz resztę swojego genomu za pomocą jednego badania.
Od 449 $Bezpłatna wysyłka · Wyniki w ciągu 6–8 tygodni
Zamawiam Genome Test137 genów powiązanych z Abnormal full-field electroretinogram
Zmiany w tych genach powodują rzadkie choroby, w których występuje Abnormal full-field electroretinogram. Większość osób z tą cechą nie ma żadnej z tych chorób, a gen z tej listy nic nie mówi o czyimkolwiek własnym genomie.
| Gen | Jak często występuje | Choroby |
|---|---|---|
| ABCA4ATP binding cassette subfamily A member 4 | Często (30–79%) | W 2 chorobach |
| ADAM9ADAM metallopeptidase domain 9 | Często (30–79%) | W 1 chorobie |
| AGBL5AGBL carboxypeptidase 5 | Często (30–79%) | W 1 chorobie |
| AHI1Abelson helper integration site 1 | Często (30–79%) | W 1 chorobie |
| AHRaryl hydrocarbon receptor | Często (30–79%) | W 1 chorobie |
| AIPL1AIP like 1 HSP90 co-chaperone | Często (30–79%) | W 2 chorobach |
| ALMS1ALMS1 centrosome and basal body associated protein | Często (30–79%) | W 1 chorobie |
| ARHGEF18Rho/Rac guanine nucleotide exchange factor 18 | Często (30–79%) | W 1 chorobie |
| ARL2BPARF like GTPase 2 binding protein | Często (30–79%) | W 1 chorobie |
| ARL3ARF like GTPase 3 | Często (30–79%) | W 1 chorobie |
| ARL6ARF like GTPase 6 | Często (30–79%) | W 1 chorobie |
| ATF6activating transcription factor 6 | Często (30–79%) | W 1 chorobie |
| BBS1Bardet-Biedl syndrome 1 | Często (30–79%) | W 1 chorobie |
| BBS2Bardet-Biedl syndrome 2 | Często (30–79%) | W 1 chorobie |
| BEST1bestrophin 1 | Często (30–79%) | W 1 chorobie |
| CA4carbonic anhydrase 4 | Często (30–79%) | W 1 chorobie |
| CABP4calcium binding protein 4 | Często (30–79%) | W 1 chorobie |
| CACNA1Fcalcium voltage-gated channel subunit alpha1 F | Często (30–79%) | W 1 chorobie |
| CACNA2D4calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Często (30–79%) | W 1 chorobie |
| CC2D2Acoiled-coil and C2 domain containing 2A | Często (30–79%) | W 1 chorobie |
| CDHR1cadherin related family member 1 | Często (30–79%) | W 2 chorobach |
| CEP290centrosomal protein 290 | Często (30–79%) | W 1 chorobie |
| CERKLCERK like autophagy regulator | Często (30–79%) | W 1 chorobie |
| CFAP20cilia and flagella associated protein 20 | Często (30–79%) | W 1 chorobie |
| CFAP410cilia and flagella associated protein 410 | Często (30–79%) | W 1 chorobie |
| CFAP418cilia and flagella associated protein 418 | Często (30–79%) | W 2 chorobach |
| CLRN1clarin 1 | Często (30–79%) | W 1 chorobie |
| CNGA1cyclic nucleotide gated channel subunit alpha 1 | Często (30–79%) | W 1 chorobie |
| CNGA3cyclic nucleotide gated channel subunit alpha 3 | Często (30–79%) | W 1 chorobie |
| CNGB1cyclic nucleotide gated channel subunit beta 1 | Często (30–79%) | W 1 chorobie |
| COQ8Bcoenzyme Q8B | Często (30–79%) | W 1 chorobie |
| CRB1crumbs cell polarity complex component 1 | Często (30–79%) | W 2 chorobach |
| CRXcone-rod homeobox | Często (30–79%) | W 3 chorobach |
| DHDDSdehydrodolichyl diphosphate synthase subunit | Często (30–79%) | W 1 chorobie |
| DHX38DEAH-box helicase 38 | Często (30–79%) | W 1 chorobie |
| DRAM2DNA damage regulated autophagy modulator 2 | Często (30–79%) | W 1 chorobie |
| EYSEGF-like photoreceptor maintenance factor | Często (30–79%) | W 1 chorobie |
| FAM161AFAM161 centrosomal protein A | Często (30–79%) | W 1 chorobie |
| FOXC1forkhead box C1 | Często (30–79%) | W 1 chorobie |
| FSCN2fascin actin-bundling protein 2, retinal | Często (30–79%) | W 1 chorobie |
Pokaż jeszcze 97 genów
| Gen | Jak często występuje | Choroby |
|---|---|---|
| FSD1Lfibronectin type III and SPRY domain containing 1 like | Często (30–79%) | W 2 chorobach |
| GDF6growth differentiation factor 6 | Często (30–79%) | W 1 chorobie |
| GUCA1Aguanylate cyclase activator 1A | Często (30–79%) | W 1 chorobie |
| GUCA1Bguanylate cyclase activator 1B | Często (30–79%) | W 1 chorobie |
| GUCY2Dguanylate cyclase 2D, retinal | Często (30–79%) | W 2 chorobach |
| HGSNATheparan-alpha-glucosaminide N-acetyltransferase | Często (30–79%) | W 1 chorobie |
| HKDC1hexokinase domain containing 1 | Często (30–79%) | W 1 chorobie |
| IDH3Aisocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha | Często (30–79%) | W 1 chorobie |
| IDH3Bisocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit beta | Często (30–79%) | W 1 chorobie |
| IFT140intraflagellar transport 140 | Często (30–79%) | W 2 chorobach |
| IFT172intraflagellar transport 172 | Często (30–79%) | W 1 chorobie |
| IFT43intraflagellar transport 43 | Często (30–79%) | W 1 chorobie |
| IFT88intraflagellar transport 88 | Często (30–79%) | W 1 chorobie |
| IMPDH1inosine monophosphate dehydrogenase 1 | Często (30–79%) | W 2 chorobach |
| IMPG1interphotoreceptor matrix proteoglycan 1 | Często (30–79%) | W 1 chorobie |
| IMPG2interphotoreceptor matrix proteoglycan 2 | Często (30–79%) | W 1 chorobie |
| IQCB1IQ motif containing B1 | Często (30–79%) | W 1 chorobie |
| KCNJ13potassium inwardly rectifying channel subfamily J member 13 | Często (30–79%) | W 1 chorobie |
| KIAA1549KIAA1549 | Często (30–79%) | W 1 chorobie |
| KIZkizuna centrosomal protein | Często (30–79%) | W 1 chorobie |
| KLHL7kelch like family member 7 | Często (30–79%) | W 1 chorobie |
| LCA5lebercilin LCA5 | Często (30–79%) | W 1 chorobie |
| LRATlecithin retinol acyltransferase | Często (30–79%) | W 2 chorobach |
| MAKmale germ cell associated kinase | Często (30–79%) | W 1 chorobie |
| MERTKMER proto-oncogene, tyrosine kinase | Często (30–79%) | W 1 chorobie |
| MFSD8major facilitator superfamily domain containing 8 | Często (30–79%) | W 1 chorobie |
| NEK2NIMA related kinase 2 | Często (30–79%) | W 1 chorobie |
| NMNAT1nicotinamide nucleotide adenylyltransferase 1 | Często (30–79%) | W 2 chorobach |
| NR2E3nuclear receptor subfamily 2 group E member 3 | Często (30–79%) | W 1 chorobie |
| NRLneural retina leucine zipper | Często (30–79%) | W 1 chorobie |
| OFD1OFD1 centriole and centriolar satellite protein | Często (30–79%) | W 1 chorobie |
| OPN1LWopsin 1, long wave sensitive | Często (30–79%) | W 1 chorobie |
| OPN1MWopsin 1, medium wave sensitive | Często (30–79%) | W 1 chorobie |
| OTX2orthodenticle homeobox 2 | Często (30–79%) | W 1 chorobie |
| PAX6paired box 6 | Często (30–79%) | W 1 chorobie |
| PCAREphotoreceptor cilium actin regulator | Często (30–79%) | W 1 chorobie |
| PCYT1Aphosphate cytidylyltransferase 1A, choline | Często (30–79%) | W 1 chorobie |
| PDE6Aphosphodiesterase 6A | Często (30–79%) | W 1 chorobie |
| PDE6Bphosphodiesterase 6B | Często (30–79%) | W 1 chorobie |
| PDE6Gphosphodiesterase 6G | Często (30–79%) | W 1 chorobie |
| PITPNM3PITPNM family member 3 | Często (30–79%) | W 1 chorobie |
| POC1BPOC1 centriolar protein B | Często (30–79%) | W 1 chorobie |
| POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Często (30–79%) | W 1 chorobie |
| PRCDphotoreceptor disc component | Często (30–79%) | W 1 chorobie |
| PROM1prominin 1 | Często (30–79%) | W 2 chorobach |
| PRPF3pre-mRNA processing factor 3 | Często (30–79%) | W 1 chorobie |
| PRPF31pre-mRNA processing factor 31 | Często (30–79%) | W 1 chorobie |
| PRPF4pre-mRNA splicing tri-snRNP complex factor PRPF4 | Często (30–79%) | W 1 chorobie |
| PRPF6pre-mRNA processing factor 6 | Często (30–79%) | W 1 chorobie |
| PRPF8pre-mRNA processing factor 8 | Często (30–79%) | W 1 chorobie |
| PRPH2peripherin 2 | Często (30–79%) | W 3 chorobach |
| RAB28RAB28, member RAS oncogene family | Często (30–79%) | W 1 chorobie |
| RAX2retina and anterior neural fold homeobox 2 | Często (30–79%) | W 1 chorobie |
| RBP3retinol binding protein 3 | Często (30–79%) | W 1 chorobie |
| RD3RD3 regulator of GUCY2D | Często (30–79%) | W 1 chorobie |
| RDH12retinol dehydrogenase 12 | Często (30–79%) | W 2 chorobach |
| REEP6receptor accessory protein 6 | Często (30–79%) | W 1 chorobie |
| RGRretinal G protein coupled receptor | Często (30–79%) | W 1 chorobie |
| RHOrhodopsin | Często (30–79%) | W 1 chorobie |
| RIMS1regulating synaptic membrane exocytosis 1 | Często (30–79%) | W 1 chorobie |
| RLBP1retinaldehyde binding protein 1 | Często (30–79%) | W 1 chorobie |
| RNU4-2RNA, U4 small nuclear 2 | Często (30–79%) | W 1 chorobie |
| RNU6-1RNA, U6 small nuclear 1 | Często (30–79%) | W 1 chorobie |
| RNU6-2RNA, U6 small nuclear 2 | Często (30–79%) | W 1 chorobie |
| RNU6-8RNA, U6 small nuclear 8 | Często (30–79%) | W 1 chorobie |
| RNU6-9RNA, U6 small nuclear 9 | Często (30–79%) | W 1 chorobie |
| ROM1retinal outer segment membrane protein 1 | Często (30–79%) | W 1 chorobie |
| RP1RP1 axonemal microtubule associated | Często (30–79%) | W 1 chorobie |
| RP1L1RP1 like 1 | Często (30–79%) | W 1 chorobie |
| RP2RP2 activator of ARL3 GTPase | Często (30–79%) | W 1 chorobie |
| RP9RP9 pre-mRNA splicing factor | Często (30–79%) | W 1 chorobie |
| RPE65retinoid isomerohydrolase RPE65 | Często (30–79%) | W 2 chorobach |
| RPGRretinitis pigmentosa GTPase regulator | Często (30–79%) | W 2 chorobach |
| RPGRIP1RPGR interacting protein 1 | Często (30–79%) | W 2 chorobach |
| SAGS-antigen visual arrestin | Często (30–79%) | W 1 chorobie |
| SAXO6stabilizer of axonemal microtubules 6 | Często (30–79%) | W 1 chorobie |
| SCAPERS-phase cyclin A associated protein in the ER | Często (30–79%) | W 1 chorobie |
| SEMA4Asemaphorin 4A | Często (30–79%) | W 2 chorobach |
| SLC7A14solute carrier family 7 member 14 | Często (30–79%) | W 1 chorobie |
| SNRNP200small nuclear ribonucleoprotein U5 subunit 200 | Często (30–79%) | W 1 chorobie |
| SPATA7spermatogenesis associated 7 | Często (30–79%) | W 2 chorobach |
| TLCD3BTLC domain containing 3B | Często (30–79%) | W 1 chorobie |
| TMEM216transmembrane protein 216 | Często (30–79%) | W 1 chorobie |
| TOPORSTOP1 binding arginine/serine rich protein, E3 ubiquitin ligase | Często (30–79%) | W 1 chorobie |
| TRIM44TRIM family member 44 | Często (30–79%) | W 1 chorobie |
| TTC8tetratricopeptide repeat domain 8 | Często (30–79%) | W 1 chorobie |
| TTLL5tubulin tyrosine ligase like 5 | Często (30–79%) | W 1 chorobie |
| TUBTUB bipartite transcription factor | Często (30–79%) | W 1 chorobie |
| TUBB4Btubulin beta 4B class IVb | Często (30–79%) | W 1 chorobie |
| TULP1TUB like protein 1 | Często (30–79%) | W 2 chorobach |
| UBAP1Lubiquitin associated protein 1 like | Często (30–79%) | W 1 chorobie |
| UNC119unc-119 lipid binding chaperone | Często (30–79%) | W 1 chorobie |
| USH2Ausherin | Często (30–79%) | W 1 chorobie |
| USP45ubiquitin specific peptidase 45 | Często (30–79%) | W 1 chorobie |
| VCANversican | Często (30–79%) | W 1 chorobie |
| ZNF408zinc finger protein 408 | Często (30–79%) | W 1 chorobie |
| ZNF513zinc finger protein 513 | Często (30–79%) | W 1 chorobie |
Jak często występuje wśród osób z jedną z chorób związanych z tym genem, najczęściej spośród wszystkich, według danych Human Phenotype Ontology. Te strony opisują cechy i badania, na których się opierają; nie są diagnozą, a w sprawie objawów należy zwrócić się do lekarza lub doradcy genetycznego.
Cechy podrzędne
Cechy nadrzędne
Skąd pochodzą te dane
- Human Phenotype Ontology, wydanie 2026-09-01: cecha, jej nazwy, definicja oraz geny z nią powiązane. Więcej informacji znajdą Państwo na stronie hpo.jax.org.
- Wydanie danych 2026.10.19-9814e911.
AtlasDla kogo jest Dante LabsNasza naukaProduktyWyniki
Zaloguj sięZapytajZsekwencjonuj swój genom↗
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 810+ physician-ready reports.
Od 449 $
Bezpłatna wysyłka · Wyniki w ciągu 6–8 tygodni
