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Požymis
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.
Santrauka
- Kūno sistema
- Abnormality of the eye
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page$trait$nameAbnormal full-field electroretinogramHP:0030466
AtlasKam mes padedameMūsų mokslasProduktaiRezultatai
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Vienu tyrimu sužinokite genus, susijusius su Abnormal full-field electroretinogram, ir kitą jūsų genomo dalį.
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Įsigyti savo 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 →
Vienu tyrimu sužinokite genus, susijusius su Abnormal full-field electroretinogram, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test137 genų susiję su Abnormal full-field electroretinogram
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Abnormal full-field electroretinogram. 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 |
|---|---|---|
| ABCA4ATP binding cassette subfamily A member 4 | Dažnai (30–79%) | 2 ligose |
| ADAM9ADAM metallopeptidase domain 9 | Dažnai (30–79%) | 1 ligoje |
| AGBL5AGBL carboxypeptidase 5 | Dažnai (30–79%) | 1 ligoje |
| AHI1Abelson helper integration site 1 | Dažnai (30–79%) | 1 ligoje |
| AHRaryl hydrocarbon receptor | Dažnai (30–79%) | 1 ligoje |
| AIPL1AIP like 1 HSP90 co-chaperone | Dažnai (30–79%) | 2 ligose |
| ALMS1ALMS1 centrosome and basal body associated protein | Dažnai (30–79%) | 1 ligoje |
| ARHGEF18Rho/Rac guanine nucleotide exchange factor 18 | Dažnai (30–79%) | 1 ligoje |
| ARL2BPARF like GTPase 2 binding protein | Dažnai (30–79%) | 1 ligoje |
| ARL3ARF like GTPase 3 | Dažnai (30–79%) | 1 ligoje |
| ARL6ARF like GTPase 6 | Dažnai (30–79%) | 1 ligoje |
| ATF6activating transcription factor 6 | Dažnai (30–79%) | 1 ligoje |
| BBS1Bardet-Biedl syndrome 1 | Dažnai (30–79%) | 1 ligoje |
| BBS2Bardet-Biedl syndrome 2 | Dažnai (30–79%) | 1 ligoje |
| BEST1bestrophin 1 | Dažnai (30–79%) | 1 ligoje |
| CA4carbonic anhydrase 4 | Dažnai (30–79%) | 1 ligoje |
| CABP4calcium binding protein 4 | Dažnai (30–79%) | 1 ligoje |
| CACNA1Fcalcium voltage-gated channel subunit alpha1 F | Dažnai (30–79%) | 1 ligoje |
| CACNA2D4calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Dažnai (30–79%) | 1 ligoje |
| CC2D2Acoiled-coil and C2 domain containing 2A | Dažnai (30–79%) | 1 ligoje |
| CDHR1cadherin related family member 1 | Dažnai (30–79%) | 2 ligose |
| CEP290centrosomal protein 290 | Dažnai (30–79%) | 1 ligoje |
| CERKLCERK like autophagy regulator | Dažnai (30–79%) | 1 ligoje |
| CFAP20cilia and flagella associated protein 20 | Dažnai (30–79%) | 1 ligoje |
| CFAP410cilia and flagella associated protein 410 | Dažnai (30–79%) | 1 ligoje |
| CFAP418cilia and flagella associated protein 418 | Dažnai (30–79%) | 2 ligose |
| CLRN1clarin 1 | Dažnai (30–79%) | 1 ligoje |
| CNGA1cyclic nucleotide gated channel subunit alpha 1 | Dažnai (30–79%) | 1 ligoje |
| CNGA3cyclic nucleotide gated channel subunit alpha 3 | Dažnai (30–79%) | 1 ligoje |
| CNGB1cyclic nucleotide gated channel subunit beta 1 | Dažnai (30–79%) | 1 ligoje |
| COQ8Bcoenzyme Q8B | Dažnai (30–79%) | 1 ligoje |
| CRB1crumbs cell polarity complex component 1 | Dažnai (30–79%) | 2 ligose |
| CRXcone-rod homeobox | Dažnai (30–79%) | 3 ligose |
| DHDDSdehydrodolichyl diphosphate synthase subunit | Dažnai (30–79%) | 1 ligoje |
| DHX38DEAH-box helicase 38 | Dažnai (30–79%) | 1 ligoje |
| DRAM2DNA damage regulated autophagy modulator 2 | Dažnai (30–79%) | 1 ligoje |
| EYSEGF-like photoreceptor maintenance factor | Dažnai (30–79%) | 1 ligoje |
| FAM161AFAM161 centrosomal protein A | Dažnai (30–79%) | 1 ligoje |
| FOXC1forkhead box C1 | Dažnai (30–79%) | 1 ligoje |
| FSCN2fascin actin-bundling protein 2, retinal | Dažnai (30–79%) | 1 ligoje |
Rodyti dar 97 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| FSD1Lfibronectin type III and SPRY domain containing 1 like | Dažnai (30–79%) | 2 ligose |
| GDF6growth differentiation factor 6 | Dažnai (30–79%) | 1 ligoje |
| GUCA1Aguanylate cyclase activator 1A | Dažnai (30–79%) | 1 ligoje |
| GUCA1Bguanylate cyclase activator 1B | Dažnai (30–79%) | 1 ligoje |
| GUCY2Dguanylate cyclase 2D, retinal | Dažnai (30–79%) | 2 ligose |
| HGSNATheparan-alpha-glucosaminide N-acetyltransferase | Dažnai (30–79%) | 1 ligoje |
| HKDC1hexokinase domain containing 1 | Dažnai (30–79%) | 1 ligoje |
| IDH3Aisocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha | Dažnai (30–79%) | 1 ligoje |
| IDH3Bisocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit beta | Dažnai (30–79%) | 1 ligoje |
| IFT140intraflagellar transport 140 | Dažnai (30–79%) | 2 ligose |
| IFT172intraflagellar transport 172 | Dažnai (30–79%) | 1 ligoje |
| IFT43intraflagellar transport 43 | Dažnai (30–79%) | 1 ligoje |
| IFT88intraflagellar transport 88 | Dažnai (30–79%) | 1 ligoje |
| IMPDH1inosine monophosphate dehydrogenase 1 | Dažnai (30–79%) | 2 ligose |
| IMPG1interphotoreceptor matrix proteoglycan 1 | Dažnai (30–79%) | 1 ligoje |
| IMPG2interphotoreceptor matrix proteoglycan 2 | Dažnai (30–79%) | 1 ligoje |
| IQCB1IQ motif containing B1 | Dažnai (30–79%) | 1 ligoje |
| KCNJ13potassium inwardly rectifying channel subfamily J member 13 | Dažnai (30–79%) | 1 ligoje |
| KIAA1549KIAA1549 | Dažnai (30–79%) | 1 ligoje |
| KIZkizuna centrosomal protein | Dažnai (30–79%) | 1 ligoje |
| KLHL7kelch like family member 7 | Dažnai (30–79%) | 1 ligoje |
| LCA5lebercilin LCA5 | Dažnai (30–79%) | 1 ligoje |
| LRATlecithin retinol acyltransferase | Dažnai (30–79%) | 2 ligose |
| MAKmale germ cell associated kinase | Dažnai (30–79%) | 1 ligoje |
| MERTKMER proto-oncogene, tyrosine kinase | Dažnai (30–79%) | 1 ligoje |
| MFSD8major facilitator superfamily domain containing 8 | Dažnai (30–79%) | 1 ligoje |
| NEK2NIMA related kinase 2 | Dažnai (30–79%) | 1 ligoje |
| NMNAT1nicotinamide nucleotide adenylyltransferase 1 | Dažnai (30–79%) | 2 ligose |
| NR2E3nuclear receptor subfamily 2 group E member 3 | Dažnai (30–79%) | 1 ligoje |
| NRLneural retina leucine zipper | Dažnai (30–79%) | 1 ligoje |
| OFD1OFD1 centriole and centriolar satellite protein | Dažnai (30–79%) | 1 ligoje |
| OPN1LWopsin 1, long wave sensitive | Dažnai (30–79%) | 1 ligoje |
| OPN1MWopsin 1, medium wave sensitive | Dažnai (30–79%) | 1 ligoje |
| OTX2orthodenticle homeobox 2 | Dažnai (30–79%) | 1 ligoje |
| PAX6paired box 6 | Dažnai (30–79%) | 1 ligoje |
| PCAREphotoreceptor cilium actin regulator | Dažnai (30–79%) | 1 ligoje |
| PCYT1Aphosphate cytidylyltransferase 1A, choline | Dažnai (30–79%) | 1 ligoje |
| PDE6Aphosphodiesterase 6A | Dažnai (30–79%) | 1 ligoje |
| PDE6Bphosphodiesterase 6B | Dažnai (30–79%) | 1 ligoje |
| PDE6Gphosphodiesterase 6G | Dažnai (30–79%) | 1 ligoje |
| PITPNM3PITPNM family member 3 | Dažnai (30–79%) | 1 ligoje |
| POC1BPOC1 centriolar protein B | Dažnai (30–79%) | 1 ligoje |
| POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Dažnai (30–79%) | 1 ligoje |
| PRCDphotoreceptor disc component | Dažnai (30–79%) | 1 ligoje |
| PROM1prominin 1 | Dažnai (30–79%) | 2 ligose |
| PRPF3pre-mRNA processing factor 3 | Dažnai (30–79%) | 1 ligoje |
| PRPF31pre-mRNA processing factor 31 | Dažnai (30–79%) | 1 ligoje |
| PRPF4pre-mRNA splicing tri-snRNP complex factor PRPF4 | Dažnai (30–79%) | 1 ligoje |
| PRPF6pre-mRNA processing factor 6 | Dažnai (30–79%) | 1 ligoje |
| PRPF8pre-mRNA processing factor 8 | Dažnai (30–79%) | 1 ligoje |
| PRPH2peripherin 2 | Dažnai (30–79%) | 3 ligose |
| RAB28RAB28, member RAS oncogene family | Dažnai (30–79%) | 1 ligoje |
| RAX2retina and anterior neural fold homeobox 2 | Dažnai (30–79%) | 1 ligoje |
| RBP3retinol binding protein 3 | Dažnai (30–79%) | 1 ligoje |
| RD3RD3 regulator of GUCY2D | Dažnai (30–79%) | 1 ligoje |
| RDH12retinol dehydrogenase 12 | Dažnai (30–79%) | 2 ligose |
| REEP6receptor accessory protein 6 | Dažnai (30–79%) | 1 ligoje |
| RGRretinal G protein coupled receptor | Dažnai (30–79%) | 1 ligoje |
| RHOrhodopsin | Dažnai (30–79%) | 1 ligoje |
| RIMS1regulating synaptic membrane exocytosis 1 | Dažnai (30–79%) | 1 ligoje |
| RLBP1retinaldehyde binding protein 1 | Dažnai (30–79%) | 1 ligoje |
| RNU4-2RNA, U4 small nuclear 2 | Dažnai (30–79%) | 1 ligoje |
| RNU6-1RNA, U6 small nuclear 1 | Dažnai (30–79%) | 1 ligoje |
| RNU6-2RNA, U6 small nuclear 2 | Dažnai (30–79%) | 1 ligoje |
| RNU6-8RNA, U6 small nuclear 8 | Dažnai (30–79%) | 1 ligoje |
| RNU6-9RNA, U6 small nuclear 9 | Dažnai (30–79%) | 1 ligoje |
| ROM1retinal outer segment membrane protein 1 | Dažnai (30–79%) | 1 ligoje |
| RP1RP1 axonemal microtubule associated | Dažnai (30–79%) | 1 ligoje |
| RP1L1RP1 like 1 | Dažnai (30–79%) | 1 ligoje |
| RP2RP2 activator of ARL3 GTPase | Dažnai (30–79%) | 1 ligoje |
| RP9RP9 pre-mRNA splicing factor | Dažnai (30–79%) | 1 ligoje |
| RPE65retinoid isomerohydrolase RPE65 | Dažnai (30–79%) | 2 ligose |
| RPGRretinitis pigmentosa GTPase regulator | Dažnai (30–79%) | 2 ligose |
| RPGRIP1RPGR interacting protein 1 | Dažnai (30–79%) | 2 ligose |
| SAGS-antigen visual arrestin | Dažnai (30–79%) | 1 ligoje |
| SAXO6stabilizer of axonemal microtubules 6 | Dažnai (30–79%) | 1 ligoje |
| SCAPERS-phase cyclin A associated protein in the ER | Dažnai (30–79%) | 1 ligoje |
| SEMA4Asemaphorin 4A | Dažnai (30–79%) | 2 ligose |
| SLC7A14solute carrier family 7 member 14 | Dažnai (30–79%) | 1 ligoje |
| SNRNP200small nuclear ribonucleoprotein U5 subunit 200 | Dažnai (30–79%) | 1 ligoje |
| SPATA7spermatogenesis associated 7 | Dažnai (30–79%) | 2 ligose |
| TLCD3BTLC domain containing 3B | Dažnai (30–79%) | 1 ligoje |
| TMEM216transmembrane protein 216 | Dažnai (30–79%) | 1 ligoje |
| TOPORSTOP1 binding arginine/serine rich protein, E3 ubiquitin ligase | Dažnai (30–79%) | 1 ligoje |
| TRIM44TRIM family member 44 | Dažnai (30–79%) | 1 ligoje |
| TTC8tetratricopeptide repeat domain 8 | Dažnai (30–79%) | 1 ligoje |
| TTLL5tubulin tyrosine ligase like 5 | Dažnai (30–79%) | 1 ligoje |
| TUBTUB bipartite transcription factor | Dažnai (30–79%) | 1 ligoje |
| TUBB4Btubulin beta 4B class IVb | Dažnai (30–79%) | 1 ligoje |
| TULP1TUB like protein 1 | Dažnai (30–79%) | 2 ligose |
| UBAP1Lubiquitin associated protein 1 like | Dažnai (30–79%) | 1 ligoje |
| UNC119unc-119 lipid binding chaperone | Dažnai (30–79%) | 1 ligoje |
| USH2Ausherin | Dažnai (30–79%) | 1 ligoje |
| USP45ubiquitin specific peptidase 45 | Dažnai (30–79%) | 1 ligoje |
| VCANversican | Dažnai (30–79%) | 1 ligoje |
| ZNF408zinc finger protein 408 | Dažnai (30–79%) | 1 ligoje |
| ZNF513zinc finger protein 513 | Dažnai (30–79%) | 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.
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- 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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PrisijungtiKlaustiSekvenuokite savo genomą↗
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