AtlasKiknek segítünkTudományunkTermékekEredmények
BejelentkezésKérdezzenSzekvenálja genomját↗
Tulajdonság
Low levels of amniotic fluid
Klinikai név: Oligohydramnios
Diminished amniotic fluid volume in pregnancy.
Összefoglaló
- Más néven
- Maternal oligohydramnios
- Szervrendszer
- Abnormality of prenatal development or birth
AtlasKiknek segítünkTudományunkTermékekEredmények
BejelentkezésKérdezzenSzekvenálja genomját↗
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library(jsonlite)
url <- "https://dantelabs.com/traits/oligohydramnios.json"
page <- fromJSON(url)
page$trait$nameLow levels of amniotic fluidHP:0001562
AtlasKiknek segítünkTudományunkTermékekEredmények
BejelentkezésKérdezzenSzekvenálja genomját↗
Olvassa el a(z) Low levels of amniotic fluid nevű génhez kapcsolódó információkat, valamint a genomja többi részét egyetlen teszttel.
449 $-tólIngyenes szállítás · Eredmények 6–8 hét alatt
Kérem a Genome Testemet114 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.
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- DNA Repair DiseaseReads 18 of these genesBRCA1BRCA2BRIP1ERCC4FANCAFANCBAbout this report →
- Joubert Syndrome And Related DisordersReads 15 of these genesTMEM231TCTN3B9D1B9D2CC2D2ACEP290About this report →
Show 110 more reports
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- Hereditary Visceral Myopathy, CIPO & MMIHSReads 4 of these genesMYH11MYL9ACTG2MYLKAbout this report →
- GPI Anchor Biosynthesis DefectsReads 7 of these genesPGAP2PGAP3PIGLPIGOPIGVPIGWAbout this report →
- Polycystic Kidney DiseaseReads 5 of these genesALG8DZIP1LNEK8PKHD1ALG9About this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 3 of these genesHNF1BSEC61A1RENAbout this report →
- Congenital Disorders of GlycosylationReads 13 of these genesALG8ALG9B3GALT6COG5GMPPBPGAP2About this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 4 of these genesGFRA1GREB1LITGA8PAX2About this report →
- Fraser SyndromeReads 2 of these genesFREM2GRIP1About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 2 of these genesRETPHOX2BAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 8 of these genesTMEM231CC2D2ACEP290CSPP1MKS1TMEM216About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 3 of these genesBRIP1PALB2RAD51CAbout this report →
- ARC Syndrome 1 (VPS33B)Reads 1 of these genesVPS33BAbout this report →
- ARC Syndrome 2 (VIPAS39)Reads 1 of these genesVIPAS39About this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Congenital AnalbuminaemiaReads 1 of these genesALBAbout this report →
- Congenital Central Hypoventilation SyndromeReads 1 of these genesPHOX2BAbout this report →
- EBF3-Related Neurodevelopmental Disorder (HADDS)Reads 1 of these genesEBF3About this report →
- FANCM-Related Genomic Instability DisorderReads 1 of these genesFANCMAbout this report →
- Frontonasal Dysplasia with Alopecia and Genital Anomaly (ALX4)Reads 1 of these genesALX4About this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- Hereditary Leiomyomatosis and Renal Cell CancerReads 1 of these genesFHAbout this report →
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- NEK8-Related Renal-Hepatic-Pancreatic DysplasiaReads 1 of these genesNEK8About this report →
- OpsismodysplasiaReads 1 of these genesINPPL1About this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- PBX1-Related Kidney and Urinary Tract AnomaliesReads 1 of these genesPBX1About this report →
- PDX1-Related Pancreatic AgenesisReads 1 of these genesPDX1About this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- Stüve-Wiedemann SyndromeReads 1 of these genesLIFRAbout this report →
- TARP SyndromeReads 1 of these genesRBM10About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 4 of these genesNEK8NPHP3TMEM67INVSAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 2 of these genesHBA1HBA2About this report →
- ThalassaemiaReads 2 of these genesHBA1HBA2About this report →
- Aortic AneurysmReads 3 of these genesMYH11FBN1MYLKAbout this report →
- Cutis LaxaReads 3 of these genesEFEMP2ATP6V1E1FBLN5About this report →
- Inherited Neurodegenerative DisordersReads 14 of these genesTMEM231CC2D2ACEP290CSPP1IFIH1MKS1About this report →
- PolycythemiaReads 2 of these genesHBA1HBA2About this report →
- Red Blood Cell Membrane DisordersReads 2 of these genesRHAGRHCEAbout this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Enlarged Parietal Foramina (MSX2)Reads 1 of these genesALX4About this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A24About this report →
- Müllerian Aplasia (MRKH Syndrome)Reads 1 of these genesWNT4About this report →
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 1 of these genesPHOX2BAbout this report →
- Epidermolysis BullosaReads 3 of these genesDSTDSPJUPAbout this report →
- Neonatal Diabetes MellitusReads 3 of these genesPDX1GATA6HNF1BAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 3 of these genesTRA2BTBCKZFXAbout this report →
- Arrhythmogenic CardiomyopathyReads 2 of these genesDSPJUPAbout this report →
- Primary Mitochondrial DiseaseReads 7 of these genesUQCC2TMEM70C1QBPMTO1SFXN4NDUFA6About this report →
- Maturity-Onset Diabetes Of The YoungReads 2 of these genesPDX1HNF1BAbout this report →
- HyperthyroidismReads 1 of these genesALBAbout this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRNU4ATACAbout this report →
- Monogenic Precocious PubertyReads 1 of these genesMKRN3About this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Diabetes MellitusReads 3 of these genesPDX1GATA6HNF1BAbout this report →
- OsteopetrosisReads 2 of these genesCA2AMER1About this report →
- Intellectual DisabilityReads 8 of these genesCERT1DYRK1AHIVEP2NAA10PIGLPUF60About this report →
- Osteogenesis ImperfectaReads 3 of these genesIFIH1MBTPS2SEC24DAbout this report →
- Polycystic Liver Disease (1 and 2)Reads 1 of these genesALG8About this report →
- Mosaic Variegated Aneuploidy SyndromeReads 1 of these genesBUB1BAbout this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 2 of these genesCEP290RPGRIP1About this report →
- Bardet-Biedl and Alström SyndromesReads 2 of these genesCEP290MKS1About this report →
- Female InfertilityReads 3 of these genesLARS2WNT4FANCMAbout this report →
- Adams-Oliver SyndromeReads 1 of these genesDOCK6About this report →
- Hypertrophic CardiomyopathyReads 3 of these genesCDKN1CH19IGF2About this report →
- Congenital Adrenal HyperplasiaReads 1 of these genesPORAbout this report →
- Congenital Cranial Dysinnervation DisordersReads 1 of these genesCOL25A1About this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesDEF6About this report →
- Congenital Muscular DystrophiesReads 2 of these genesTRIP4GMPPBAbout this report →
- Thyroid CancerReads 2 of these genesRETALBAbout this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesIFIH1About this report →
- GlomerulosclerosisReads 1 of these genesPAX2About this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesHSPA9About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesRETAbout this report →
- Pyruvate Kinase Deficiency and Other Red Cell Enzyme DisordersReads 1 of these genesTPI1About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 2 of these genesDSPMBTPS2About this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 1 of these genesSEC61A1About this report →
- Focal Segmental GlomerulosclerosisReads 1 of these genesPAX2About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesRETAbout this report →
- Marfan Like SyndromesReads 1 of these genesFBN1About this report →
- Coffin-Siris SyndromeReads 1 of these genesDPF2About this report →
- LipodystrophyReads 1 of these genesZMPSTE24About this report →
- Type I InterferonopathiesReads 1 of these genesIFIH1About this report →
- Urinary and Renal System TumourReads 1 of these genesRETAbout this report →
- Hypogonadotropic HypogonadismReads 2 of these genesMAGEL2SNRPNAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesGATA6About this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesDSTFHCOQ7FBLN5About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesCPT2About this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesKIF14About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesCOQ7FBLN5About this report →
- Congenital MyopathiesReads 1 of these genesBIN1About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesB3GALT6About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesDSTAbout this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesEXOSC9About this report →
- Syndromic CraniosynostosisReads 1 of these genesPORAbout this report →
- Other Inborn Errors of ImmunityReads 3 of these genesDEF6IFIH1SEC61A1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesGLI3About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesGMPPBAbout this report →
- Nephrotic SyndromeReads 1 of these genesLAMB2About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesGMPPBAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesIFIH1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesATN1About this report →
- Male InfertilityReads 1 of these genesFANCMAbout this report →
- Epilepsy (Full Panel)Reads 2 of these genesSZT2SLC35A2About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGNPTABAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesIFIH1About this report →
- Retinitis PigmentosaReads 1 of these genesCC2D2AAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesGREB1LAbout this report →
Olvassa el a(z) Low levels of amniotic fluid nevű génhez kapcsolódó információkat, valamint a genomja többi részét egyetlen teszttel.
449 $-tólIngyenes szállítás · Eredmények 6–8 hét alatt
Kérem a Genome Testemet209 gén kapcsolódik ehhez: Low levels of amniotic fluid
Ezeknek a géneknek a változásai olyan ritka betegségeket okoznak, amelyekben előfordul a(z) Low levels of amniotic fluid. A tulajdonsággal rendelkező emberek többségének nincs ezek közül egyik betegsége sem, a listán szereplő gének pedig semmit nem mondanak el senki saját genomjáról.
| Gén | Milyen gyakran fordul elő | Betegségek |
|---|---|---|
| BNIP1BCL2 interacting protein 1 | Mindig | 1 betegségben |
| CEP55centrosomal protein 55 | Mindig | 1 betegségben |
| COX14cytochrome c oxidase assembly factor COX14 | Mindig | 1 betegségben |
| DALRD3DALR anticodon binding domain containing 3 | Mindig | 1 betegségben |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Mindig | 1 betegségben |
| EXOC3L2exocyst complex component 3 like 2 | Mindig | 1 betegségben |
| FARSAphenylalanyl-tRNA synthetase subunit alpha | Mindig | 1 betegségben |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Mindig | 1 betegségben |
| IARS1isoleucyl-tRNA synthetase 1 | Mindig | 2 betegségben |
| LARS2leucyl-tRNA synthetase 2, mitochondrial | Mindig | 1 betegségben |
| LRRC7leucine rich repeat containing 7 | Mindig | 1 betegségben |
| MED16mediator complex subunit 16 | Mindig | 1 betegségben |
| MYH11myosin heavy chain 11 | Mindig | 1 betegségben |
| MYL9myosin light chain 9 | Mindig | 1 betegségben |
| NDUFB7NADH:ubiquinone oxidoreductase subunit B7 | Mindig | 1 betegségben |
| PDX1pancreatic and duodenal homeobox 1 | Mindig | 1 betegségben |
| RCC1regulator of chromosome condensation 1 | Mindig | 1 betegségben |
| RNU5B-1RNA, U5B small nuclear 1 | Mindig | 1 betegségben |
| SLC25A24solute carrier family 25 member 24 | Mindig | 1 betegségben |
| TMEM231transmembrane protein 231 | Mindig | 2 betegségben |
| TRA2Btransformer 2 beta homolog | Mindig | 1 betegségben |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Mindig | 1 betegségben |
| UQCC2ubiquinol-cytochrome c reductase complex assembly factor 2 | Mindig | 1 betegségben |
| WNT4Wnt family member 4 | Mindig | 2 betegségben |
| ZMPSTE24zinc metallopeptidase STE24 | Mindig | 1 betegségben |
| FGF20fibroblast growth factor 20 | Nagyon gyakran (80–99%) | 1 betegségben |
| GFRA1GDNF family receptor alpha 1 | Nagyon gyakran (80–99%) | 1 betegségben |
| GREB1LGREB1 like retinoic acid receptor coactivator | Nagyon gyakran (80–99%) | 1 betegségben |
| HYMAIhydatidiform mole associated and imprinted | Nagyon gyakran (80–99%) | 1 betegségben |
| ITGA8integrin subunit alpha 8 | Nagyon gyakran (80–99%) | 2 betegségben |
| PLAGL1PLAG1 like zinc finger 1 | Nagyon gyakran (80–99%) | 1 betegségben |
| RETret proto-oncogene | Nagyon gyakran (80–99%) | 2 betegségben |
| TCTN3tectonic family member 3 | Nagyon gyakran (80–99%) | 2 betegségben |
| TMEM70transmembrane protein 70 | Nagyon gyakran (80–99%) | 2 betegségben |
| WNT9BWnt family member 9B | Nagyon gyakran (80–99%) | 1 betegségben |
| ACTG2actin gamma 2, smooth muscle | Gyakran (30–79%) | 1 betegségben |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Gyakran (30–79%) | 2 betegségben |
| ALX4ALX homeobox 4 | Gyakran (30–79%) | 2 betegségben |
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | Gyakran (30–79%) | 1 betegségben |
| B9D1B9 domain containing 1 | Gyakran (30–79%) | 1 betegségben |
További 169 gén megjelenítése
| Gén | Milyen gyakran fordul elő | Betegségek |
|---|---|---|
| B9D2B9 domain containing 2 | Gyakran (30–79%) | 1 betegségben |
| BIN1bridging integrator 1 | Gyakran (30–79%) | 1 betegségben |
| C1QBPcomplement C1q binding protein | Gyakran (30–79%) | 1 betegségben |
| CC2D2Acoiled-coil and C2 domain containing 2A | Gyakran (30–79%) | 1 betegségben |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Gyakran (30–79%) | 1 betegségben |
| CEP290centrosomal protein 290 | Gyakran (30–79%) | 1 betegségben |
| CERT1ceramide transporter 1 | Gyakran (30–79%) | 1 betegségben |
| CHRM3cholinergic receptor muscarinic 3 | Gyakran (30–79%) | 2 betegségben |
| CSPP1centrosome and spindle pole associated protein 1 | Gyakran (30–79%) | 1 betegségben |
| DEF6DEF6 guanine nucleotide exchange factor | Gyakran (30–79%) | 1 betegségben |
| DOCK6dedicator of cytokinesis 6 | Gyakran (30–79%) | 1 betegségben |
| DSTdystonin | Gyakran (30–79%) | 2 betegségben |
| DZIP1LDAZ interacting zinc finger protein 1 like | Gyakran (30–79%) | 1 betegségben |
| EBF3EBF transcription factor 3 | Gyakran (30–79%) | 1 betegségben |
| FREM2FRAS1 related extracellular matrix 2 | Gyakran (30–79%) | 1 betegségben |
| GRIP1glutamate receptor interacting protein 1 | Gyakran (30–79%) | 1 betegségben |
| H19H19 imprinted maternally expressed transcript | Gyakran (30–79%) | 1 betegségben |
| HBA1hemoglobin subunit alpha 1 | Gyakran (30–79%) | 1 betegségben |
| HBA2hemoglobin subunit alpha 2 | Gyakran (30–79%) | 1 betegségben |
| HMGA2high mobility group AT-hook 2 | Gyakran (30–79%) | 1 betegségben |
| IFIH1interferon induced with helicase C domain 1 | Gyakran (30–79%) | 1 betegségben |
| IGF2insulin like growth factor 2 | Gyakran (30–79%) | 3 betegségben |
| KIF14kinesin family member 14 | Gyakran (30–79%) | 1 betegségben |
| LAMB2laminin subunit beta 2 | Gyakran (30–79%) | 2 betegségben |
| LIFRLIF receptor subunit alpha | Gyakran (30–79%) | 2 betegségben |
| MKS1MKS transition zone complex subunit 1 | Gyakran (30–79%) | 2 betegségben |
| MTO1mitochondrial tRNA translation optimization 1 | Gyakran (30–79%) | 1 betegségben |
| NEK8NIMA related kinase 8 | Gyakran (30–79%) | 2 betegségben |
| NOTCH3notch receptor 3 | Gyakran (30–79%) | 1 betegségben |
| NPHP3nephrocystin 3 | Gyakran (30–79%) | 4 betegségben |
| PAX2paired box 2 | Gyakran (30–79%) | 1 betegségben |
| PBX1PBX homeobox 1 | Gyakran (30–79%) | 2 betegségben |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Gyakran (30–79%) | 2 betegségben |
| PLAG1PLAG1 zinc finger | Gyakran (30–79%) | 1 betegségben |
| RBM10RNA binding motif protein 10 | Gyakran (30–79%) | 1 betegségben |
| RNF2ring finger protein 2 | Gyakran (30–79%) | 1 betegségben |
| RPGRIP1RPGR interacting protein 1 | Gyakran (30–79%) | 1 betegségben |
| RPGRIP1LRPGRIP1 like | Gyakran (30–79%) | 1 betegségben |
| SFXN4sideroflexin 4 | Gyakran (30–79%) | 1 betegségben |
| SV2Asynaptic vesicle glycoprotein 2A | Gyakran (30–79%) | 1 betegségben |
| SZT2SZT2 subunit of KICSTOR complex | Gyakran (30–79%) | 1 betegségben |
| TCTN1tectonic family member 1 | Gyakran (30–79%) | 1 betegségben |
| TCTN2tectonic family member 2 | Gyakran (30–79%) | 1 betegségben |
| TMEM107transmembrane protein 107 | Gyakran (30–79%) | 1 betegségben |
| TMEM216transmembrane protein 216 | Gyakran (30–79%) | 1 betegségben |
| TMEM237transmembrane protein 237 | Gyakran (30–79%) | 1 betegségben |
| TMEM67transmembrane protein 67 | Gyakran (30–79%) | 1 betegségben |
| TPI1triosephosphate isomerase 1 | Gyakran (30–79%) | 1 betegségben |
| TRIP4thyroid hormone receptor interactor 4 | Gyakran (30–79%) | 1 betegségben |
| TXNDC15thioredoxin domain containing 15 | Gyakran (30–79%) | 2 betegségben |
| ALBalbumin | Néha (5–29%) | 2 betegségben |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Néha (5–29%) | 2 betegségben |
| ASCL1achaete-scute family bHLH transcription factor 1 | Néha (5–29%) | 1 betegségben |
| ATN1atrophin 1 | Néha (5–29%) | 1 betegségben |
| B3GALT6beta-1,3-galactosyltransferase 6 | Néha (5–29%) | 1 betegségben |
| BRCA1BRCA1 DNA repair associated | Néha (5–29%) | 1 betegségben |
| BRCA2BRCA2 DNA repair associated | Néha (5–29%) | 1 betegségben |
| BRIP1BRCA1 interacting DNA helicase 1 | Néha (5–29%) | 1 betegségben |
| CA2carbonic anhydrase 2 | Néha (5–29%) | 1 betegségben |
| CDC42BPBCDC42 binding protein kinase beta | Néha (5–29%) | 1 betegségben |
| CLTCL1clathrin heavy chain like 1 | Néha (5–29%) | 1 betegségben |
| COG5component of oligomeric golgi complex 5 | Néha (5–29%) | 1 betegségben |
| COL25A1collagen type XXV alpha 1 chain | Néha (5–29%) | 1 betegségben |
| CPT2carnitine palmitoyltransferase 2 | Néha (5–29%) | 1 betegségben |
| CRELD1CRELD disulfide isomerase 1 | Néha (5–29%) | 1 betegségben |
| DDX6DEAD-box helicase 6 | Néha (5–29%) | 1 betegségben |
| DHPSdeoxyhypusine synthase | Néha (5–29%) | 1 betegségben |
| DPF2double PHD fingers 2 | Néha (5–29%) | 1 betegségben |
| DSPdesmoplakin | Néha (5–29%) | 1 betegségben |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Néha (5–29%) | 2 betegségben |
| ELFN1extracellular leucine rich repeat and fibronectin type III domain containing 1 | Néha (5–29%) | 1 betegségben |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Néha (5–29%) | 1 betegségben |
| ERGIC1endoplasmic reticulum-golgi intermediate compartment 1 | Néha (5–29%) | 1 betegségben |
| FAAP100FA core complex associated protein 100 | Néha (5–29%) | 1 betegségben |
| FANCAFA complementation group A | Néha (5–29%) | 1 betegségben |
| FANCBFA complementation group B | Néha (5–29%) | 1 betegségben |
| FANCCFA complementation group C | Néha (5–29%) | 1 betegségben |
| FANCD2FA complementation group D2 | Néha (5–29%) | 1 betegségben |
| FANCEFA complementation group E | Néha (5–29%) | 1 betegségben |
| FANCFFA complementation group F | Néha (5–29%) | 1 betegségben |
| FANCGFA complementation group G | Néha (5–29%) | 1 betegségben |
| FANCIFA complementation group I | Néha (5–29%) | 1 betegségben |
| FANCLFA complementation group L | Néha (5–29%) | 1 betegségben |
| FANCMFA complementation group M | Néha (5–29%) | 1 betegségben |
| FBXO22F-box protein 22 | Néha (5–29%) | 1 betegségben |
| FHfumarate hydratase | Néha (5–29%) | 1 betegségben |
| FILIP1filamin A interacting protein 1 | Néha (5–29%) | 1 betegségben |
| FRA10AC1FRA10A associated CGG repeat 1 | Néha (5–29%) | 1 betegségben |
| FXR1FMR1 autosomal homolog 1 | Néha (5–29%) | 2 betegségben |
| GATA6GATA binding protein 6 | Néha (5–29%) | 1 betegségben |
| GMPPBGDP-mannose pyrophosphorylase B | Néha (5–29%) | 1 betegségben |
| GNB2G protein subunit beta 2 | Néha (5–29%) | 1 betegségben |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Néha (5–29%) | 1 betegségben |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Néha (5–29%) | 1 betegségben |
| HIVEP2HIVEP zinc finger 2 | Néha (5–29%) | 1 betegségben |
| HNF1BHNF1 homeobox B | Néha (5–29%) | 1 betegségben |
| HS2ST1heparan sulfate 2-O-sulfotransferase 1 | Néha (5–29%) | 1 betegségben |
| INPPL1inositol polyphosphate phosphatase like 1 | Néha (5–29%) | 1 betegségben |
| JUPjunction plakoglobin | Néha (5–29%) | 1 betegségben |
| LHX1LIM homeobox 1 | Néha (5–29%) | 1 betegségben |
| MAD2L2mitotic arrest deficient 2 like 2 | Néha (5–29%) | 1 betegségben |
| MAGEL2MAGE family member L2 | Néha (5–29%) | 1 betegségben |
| MKRN3makorin ring finger protein 3 | Néha (5–29%) | 1 betegségben |
| MYH3myosin heavy chain 3 | Néha (5–29%) | 2 betegségben |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Néha (5–29%) | 1 betegségben |
| NALCNsodium leak channel, non-selective | Néha (5–29%) | 1 betegségben |
| NDUFA6NADH:ubiquinone oxidoreductase subunit A6 | Néha (5–29%) | 1 betegségben |
| NEK9NIMA related kinase 9 | Néha (5–29%) | 1 betegségben |
| NPAP1nuclear pore associated protein 1 | Néha (5–29%) | 1 betegségben |
| PALB2partner and localizer of BRCA2 | Néha (5–29%) | 1 betegségben |
| PGAP2post-GPI attachment to proteins 2 | Néha (5–29%) | 1 betegségben |
| PGAP3post-GPI attachment to proteins phospholipase 3 | Néha (5–29%) | 1 betegségben |
| PHOX2Bpaired like homeobox 2B | Néha (5–29%) | 1 betegségben |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Néha (5–29%) | 1 betegségben |
| PIGOphosphatidylinositol glycan anchor biosynthesis class O | Néha (5–29%) | 1 betegségben |
| PIGVphosphatidylinositol glycan anchor biosynthesis class V | Néha (5–29%) | 1 betegségben |
| PIGWphosphatidylinositol glycan anchor biosynthesis class W | Néha (5–29%) | 1 betegségben |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Néha (5–29%) | 1 betegségben |
| PUF60poly(U) binding splicing factor 60 | Néha (5–29%) | 1 betegségben |
| PWAR1Prader Willi/Angelman region RNA 1 | Néha (5–29%) | 1 betegségben |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Néha (5–29%) | 1 betegségben |
| RAD51RAD51 recombinase | Néha (5–29%) | 1 betegségben |
| RAD51CRAD51 paralog C | Néha (5–29%) | 1 betegségben |
| RFWD3ring finger and WD repeat domain 3 | Néha (5–29%) | 1 betegségben |
| RHAGRh associated glycoprotein | Néha (5–29%) | 1 betegségben |
| RHCERh blood group CcEe antigens | Néha (5–29%) | 1 betegségben |
| RHDRh blood group D antigen | Néha (5–29%) | 1 betegségben |
| SATB1SATB homeobox 1 | Néha (5–29%) | 1 betegségben |
| SCYL2SCY1 like pseudokinase 2 | Néha (5–29%) | 1 betegségben |
| SEC61A1SEC61 translocon subunit alpha 1 | Néha (5–29%) | 1 betegségben |
| SETD1ASET domain containing 1A, histone lysine methyltransferase | Néha (5–29%) | 1 betegségben |
| SLC35A2solute carrier family 35 member A2 | Néha (5–29%) | 1 betegségben |
| SLX4SLX4 structure-specific endonuclease subunit | Néha (5–29%) | 1 betegségben |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Néha (5–29%) | 1 betegségben |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Néha (5–29%) | 1 betegségben |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Néha (5–29%) | 1 betegségben |
| TBCKTBC1 domain containing kinase | Néha (5–29%) | 2 betegségben |
| UBE2Aubiquitin conjugating enzyme E2 A | Néha (5–29%) | 1 betegségben |
| UBE2Tubiquitin conjugating enzyme E2 T | Néha (5–29%) | 1 betegségben |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Néha (5–29%) | 1 betegségben |
| VPS33BVPS33B late endosome and lysosome associated | Néha (5–29%) | 2 betegségben |
| WBP4WW domain binding protein 4 | Néha (5–29%) | 1 betegségben |
| WSB2WD repeat and SOCS box containing 2 | Néha (5–29%) | 1 betegségben |
| XRCC2X-ray repair cross complementing 2 | Néha (5–29%) | 1 betegségben |
| ZFXzinc finger protein X-linked | Néha (5–29%) | 1 betegségben |
| BNC2basonuclin zinc finger protein 2 | Ritkán (1–4%) | 1 betegségben |
| DONSONDNA replication fork stabilization factor DONSON | Ritkán (1–4%) | 2 betegségben |
| GLI3GLI family zinc finger 3 | Ritkán (1–4%) | 1 betegségben |
| ACEangiotensin I converting enzyme | Nincs rögzítve | 1 betegségben |
| AGTangiotensinogen | Nincs rögzítve | 1 betegségben |
| AGTR1angiotensin II receptor type 1 | Nincs rögzítve | 1 betegségben |
| AMER1APC membrane recruitment protein 1 | Nincs rögzítve | 1 betegségben |
| BMPERBMP binding endothelial regulator | Nincs rögzítve | 1 betegségben |
| BUB1BBUB1 mitotic checkpoint serine/threonine kinase B | Nincs rögzítve | 1 betegségben |
| COQ7coenzyme Q7, hydroxylase | Nincs rögzítve | 1 betegségben |
| EXOSC9exosome component 9 | Nincs rögzítve | 1 betegségben |
| FBLN5fibulin 5 | Nincs rögzítve | 1 betegségben |
| FBN1fibrillin 1 | Nincs rögzítve | 1 betegségben |
| HSPA9heat shock protein family A (Hsp70) member 9 | Nincs rögzítve | 1 betegségben |
| INVSinversin | Nincs rögzítve | 1 betegségben |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Nincs rögzítve | 1 betegségben |
| MYLKmyosin light chain kinase | Nincs rögzítve | 1 betegségben |
| OSGEPO-sialoglycoprotein endopeptidase | Nincs rögzítve | 1 betegségben |
| PORcytochrome p450 oxidoreductase | Nincs rögzítve | 1 betegségben |
| RENrenin | Nincs rögzítve | 1 betegségben |
| RNU4ATACRNA, U4atac small nuclear | Nincs rögzítve | 1 betegségben |
| SEC24DSEC24 homolog D, COPII component | Nincs rögzítve | 1 betegségben |
| TALDO1transaldolase 1 | Nincs rögzítve | 1 betegségben |
| WDR73WD repeat domain 73 | Nincs rögzítve | 1 betegségben |
Az, hogy milyen gyakran fordul elő a gén valamelyik állapotával élő emberek körében (a leggyakoribb érték, ahogyan a Human Phenotype Ontology rögzíti). Ezek az oldalak tulajdonságokat és az azok mögött álló kutatásokat ismertetik; nem diagnózist jelentenek. A tünetekkel kapcsolatban orvoshoz vagy genetikai tanácsadóhoz érdemes fordulni.
Tágabb tulajdonságok
Forrás
- Human Phenotype Ontology, 2026-09-01 kiadás: a tulajdonság, a nevei, a definíciója és a hozzá kapcsolt gének. További információ: hpo.jax.org.
- Adatkiadás: 2026.10.21-311f020e.
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