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Zaloguj sięZapytajZsekwencjonuj swój genom↗
Cecha
Dental crowding
Changes in alignment of teeth in the dental arch
Podsumowanie
- Znana także jako
- Crowded teeth, Dental overcrowding, Overcrowding of teeth, Tooth size discrepancy
- Układ organizmu
- Abnormality of head or neck
AtlasKomu pomagamyNasza naukaProduktyWyniki
Zaloguj sięZapytajZsekwencjonuj swój genom↗
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/dental-crowding.json"
page <- fromJSON(url)
page$trait$nameDental crowdingHP:0000678
AtlasKomu pomagamyNasza naukaProduktyWyniki
Zaloguj sięZapytajZsekwencjonuj swój genom↗
Odczytaj geny powiązane z Dental crowding oraz resztę swojego genomu za pomocą jednego badania.
Od 449 $Bezpłatna wysyłka · Wyniki w ciągu 6–8 tygodni
Zamawiam Genome Test85 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.
- Bardet-Biedl and Alström SyndromesReads 22 of these genesBBS2ARL6BBIP1BBS1BBS10BBS12About this report →
- Intellectual DisabilityReads 27 of these genesCREBBPEP300HNRNPH1NONOSATB2SMSAbout this report →
- Fraser SyndromeReads 3 of these genesFRAS1FREM2GRIP1About this report →
- Ehlers-Danlos SyndromeReads 6 of these genesDSECOL1A2ADAMTS2COL5A1COL3A1PLOD1About this report →
Show 81 more reports
- Familial Periodic ParalysisReads 2 of these genesKCNJ2SCN4AAbout this report →
- Congenital MyopathiesReads 5 of these genesACTA1MAP3K20SELENONTPM2TPM3About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 3 of these genesNSD1H19IGF2About this report →
- 3MC Syndrome 1 (MASP1)Reads 1 of these genesMASP1About this report →
- Auriculocondylar Syndrome 2 (PLCB4)Reads 1 of these genesPLCB4About this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- Birt-Hogg-Dubé SyndromeReads 1 of these genesFLCNAbout this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- KIDINS220-Related Ventriculomegaly and ArthrogryposisReads 1 of these genesKIDINS220About this report →
- Lamb-Shaffer SyndromeReads 1 of these genesSOX5About this report →
- MDPL SyndromeReads 1 of these genesPOLD1About this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- Mulibrey NanismReads 1 of these genesTRIM37About this report →
- Radio-Tartaglia SyndromeReads 1 of these genesSPENAbout this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- Spondylo-Meta-Epiphyseal Dysplasia, Short Limb-Abnormal Calcification TypeReads 1 of these genesDDR2About this report →
- Stankiewicz-Isidor SyndromeReads 1 of these genesPSMD12About this report →
- Turnpenny-Fry SyndromeReads 1 of these genesPCGF2About this report →
- Carey-Fineman-Ziter SyndromeReads 1 of these genesMYMXAbout this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Dent Disease and Lowe SyndromeReads 1 of these genesOCRLAbout this report →
- Inherited ArthropathiesReads 1 of these genesANKHAbout this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesINSRAbout this report →
- Marfan Like SyndromesReads 2 of these genesSMAD2FBN1About this report →
- Syndromic CraniosynostosisReads 3 of these genesFGFR2IL11RAFGFR1About this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Retinitis PigmentosaReads 5 of these genesBBS2ARL6CFAP418IFT172TTC8About this report →
- Aortic AneurysmReads 2 of these genesFBN1LOXAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 4 of these genesCEP290MKS1SNX14PEX6About this report →
- Hypertrophic CardiomyopathyReads 4 of these genesNSD1H19IGF2MYL2About this report →
- Cutis LaxaReads 2 of these genesATP6V1E1EFEMP1About this report →
- Familial Atrial FibrillationReads 1 of these genesKCNJ2About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- Short Qt SyndromeReads 1 of these genesKCNJ2About this report →
- Joubert Syndrome And Related DisordersReads 3 of these genesCEP290MKS1NPHP1About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 2 of these genesNPHP1SDCCAG8About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesNEDD4LAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 2 of these genesSETD5ZFXAbout this report →
- Cornelia de Lange SyndromeReads 1 of these genesSMC1AAbout this report →
- Loeys-Dietz SyndromeReads 1 of these genesSMAD2About this report →
- Colorectal Cancer & PolyposisReads 1 of these genesPOLD1About this report →
- Hyper-IgE SyndromeReads 1 of these genesIL6STAbout this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesCEP19About this report →
- Congenital Muscular DystrophiesReads 2 of these genesITGA7SELENONAbout this report →
- Inherited Neurodegenerative DisordersReads 7 of these genesTECPR2CEP290KIDINS220MKS1NKX6-2SNX14About this report →
- GlaucomaReads 1 of these genesEFEMP1About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesLMNATRIM32About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesXYLT1About this report →
- Kidney CancerReads 1 of these genesFLCNAbout this report →
- Hereditary Macular DystrophiesReads 1 of these genesEFEMP1About this report →
- Long QT SyndromeReads 1 of these genesKCNJ2About this report →
- Meckel SyndromeReads 1 of these genesMKS1About this report →
- HyperinsulinismReads 1 of these genesINSRAbout this report →
- Epilepsy (Full Panel)Reads 4 of these genesSMC1AUPF3BZEB2IL1RAPL1About this report →
- Coffin-Siris SyndromeReads 1 of these genesARID2About this report →
- Urinary and Renal System TumourReads 1 of these genesFLCNAbout this report →
- OsteopetrosisReads 1 of these genesAMER1About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX6About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesKCNJ5About this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesTECPR2KIDINS220About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesNKX6-2PEX6About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGKAbout this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesCBSAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesTECPR2About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 1 of these genesCEP290About this report →
- Inherited IchthyosesReads 1 of these genesNSDHLAbout this report →
- Congenital Disorders of GlycosylationReads 2 of these genesDSEMGAT2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesLMNATECPR2PEX6About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesSCN4AAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesRAP1BAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesCOL1A2About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesGJA1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesSCN4AAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Hypogonadotropic HypogonadismReads 1 of these genesFGFR1About this report →
- Other Inborn Errors of ImmunityReads 2 of these genesIL6STPOLD1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
Odczytaj geny powiązane z Dental crowding oraz resztę swojego genomu za pomocą jednego badania.
Od 449 $Bezpłatna wysyłka · Wyniki w ciągu 6–8 tygodni
Zamawiam Genome Test156 genów powiązanych z Dental crowding
Zmiany w tych genach powodują rzadkie choroby, w których występuje Dental crowding. 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 |
|---|---|---|
| ARID2AT-rich interaction domain 2 | Zawsze | W 1 chorobie |
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | Zawsze | W 1 chorobie |
| BANF1barrier to autointegration nuclear assembly factor 1 | Zawsze | W 1 chorobie |
| BBS2Bardet-Biedl syndrome 2 | Zawsze | W 2 chorobach |
| CREBBPCREB binding lysine acetyltransferase | Zawsze | W 3 chorobach |
| DSEdermatan sulfate epimerase | Zawsze | W 1 chorobie |
| EMC10ER membrane protein complex subunit 10 | Zawsze | W 1 chorobie |
| EP300EP300 lysine acetyltransferase | Zawsze | W 3 chorobach |
| GNB2G protein subunit beta 2 | Zawsze | W 1 chorobie |
| HNRNPH1heterogeneous nuclear ribonucleoprotein H1 | Zawsze | W 1 chorobie |
| IL6STinterleukin 6 cytokine family signal transducer | Zawsze | W 1 chorobie |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Zawsze | W 2 chorobach |
| LGI4leucine rich repeat LGI family member 4 | Zawsze | W 1 chorobie |
| LMNAlamin A/C | Zawsze | W 2 chorobach |
| MYH3myosin heavy chain 3 | Zawsze | W 1 chorobie |
| MYMXmyomixer, myoblast fusion factor | Zawsze | W 1 chorobie |
| NONOnon-POU domain containing octamer binding | Zawsze | W 2 chorobach |
| NSD1nuclear receptor binding SET domain protein 1 | Zawsze | W 1 chorobie |
| POLD1DNA polymerase delta 1, catalytic subunit | Zawsze | W 1 chorobie |
| PTBP1polypyrimidine tract binding protein 1 | Zawsze | W 1 chorobie |
| SATB2SATB homeobox 2 | Zawsze | W 3 chorobach |
| SMC1Astructural maintenance of chromosomes 1A | Zawsze | W 1 chorobie |
| SMSspermine synthase | Zawsze | W 2 chorobach |
| TCP1t-complex 1 | Zawsze | W 1 chorobie |
| TECPR2tectonin beta-propeller repeat containing 2 | Zawsze | W 2 chorobach |
| TOMM7translocase of outer mitochondrial membrane 7 | Zawsze | W 1 chorobie |
| CBScystathionine beta-synthase | Bardzo często (80–99%) | W 2 chorobach |
| FGFR2fibroblast growth factor receptor 2 | Bardzo często (80–99%) | W 3 chorobach |
| MED12mediator complex subunit 12 | Bardzo często (80–99%) | W 4 chorobach |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Bardzo często (80–99%) | W 2 chorobach |
| SCUBE3signal peptide, CUB domain and EGF like domain containing 3 | Bardzo często (80–99%) | W 1 chorobie |
| SOBPsine oculis binding protein homolog | Bardzo często (80–99%) | W 1 chorobie |
| ABL1ABL proto-oncogene 1, non-receptor tyrosine kinase | Często (30–79%) | W 1 chorobie |
| ACTA1actin alpha 1, skeletal muscle | Często (30–79%) | W 1 chorobie |
| ADAMTS15ADAM metallopeptidase with thrombospondin type 1 motif 15 | Często (30–79%) | W 1 chorobie |
| ANKHANKH inorganic pyrophosphate transport regulator | Często (30–79%) | W 1 chorobie |
| ARL6ARF like GTPase 6 | Często (30–79%) | W 2 chorobach |
| BBIP1BBSome interacting protein 1 | Często (30–79%) | W 1 chorobie |
| BBS1Bardet-Biedl syndrome 1 | Często (30–79%) | W 2 chorobach |
| BBS10Bardet-Biedl syndrome 10 | Często (30–79%) | W 1 chorobie |
Pokaż jeszcze 116 genów
| Gen | Jak często występuje | Choroby |
|---|---|---|
| BBS12Bardet-Biedl syndrome 12 | Często (30–79%) | W 1 chorobie |
| BBS4Bardet-Biedl syndrome 4 | Często (30–79%) | W 1 chorobie |
| BBS5Bardet-Biedl syndrome 5 | Często (30–79%) | W 1 chorobie |
| BBS7Bardet-Biedl syndrome 7 | Często (30–79%) | W 1 chorobie |
| BBS9Bardet-Biedl syndrome 9 | Często (30–79%) | W 1 chorobie |
| BMP2bone morphogenetic protein 2 | Często (30–79%) | W 1 chorobie |
| CEP19centrosomal protein 19 | Często (30–79%) | W 1 chorobie |
| CEP290centrosomal protein 290 | Często (30–79%) | W 1 chorobie |
| CFAP418cilia and flagella associated protein 418 | Często (30–79%) | W 1 chorobie |
| COL1A2collagen type I alpha 2 chain | Często (30–79%) | W 1 chorobie |
| EDN1endothelin 1 | Często (30–79%) | W 1 chorobie |
| EFEMP1EGF-like fibulin extracellular matrix protein 1 | Często (30–79%) | W 1 chorobie |
| FRAS1Fraser extracellular matrix complex subunit 1 | Często (30–79%) | W 2 chorobach |
| FREM2FRAS1 related extracellular matrix 2 | Często (30–79%) | W 1 chorobie |
| GNAI3G protein subunit alpha i3 | Często (30–79%) | W 2 chorobach |
| GRIP1glutamate receptor interacting protein 1 | Często (30–79%) | W 1 chorobie |
| H19H19 imprinted maternally expressed transcript | Często (30–79%) | W 1 chorobie |
| HACD13-hydroxyacyl-CoA dehydratase 1 | Często (30–79%) | W 1 chorobie |
| IFT172intraflagellar transport 172 | Często (30–79%) | W 1 chorobie |
| IFT27intraflagellar transport 27 | Często (30–79%) | W 1 chorobie |
| IFT74intraflagellar transport 74 | Często (30–79%) | W 1 chorobie |
| IGF2insulin like growth factor 2 | Często (30–79%) | W 1 chorobie |
| IL11RAinterleukin 11 receptor subunit alpha | Często (30–79%) | W 1 chorobie |
| INSRinsulin receptor | Często (30–79%) | W 1 chorobie |
| ITGA7integrin subunit alpha 7 | Często (30–79%) | W 1 chorobie |
| KIDINS220kinase D interacting substrate 220 | Często (30–79%) | W 1 chorobie |
| LZTFL1leucine zipper transcription factor like 1 | Często (30–79%) | W 1 chorobie |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Często (30–79%) | W 1 chorobie |
| MKKSMKKS centrosomal shuttling protein | Często (30–79%) | W 1 chorobie |
| MKS1MKS transition zone complex subunit 1 | Często (30–79%) | W 1 chorobie |
| MYL2myosin light chain 2 | Często (30–79%) | W 1 chorobie |
| NOTCH3notch receptor 3 | Często (30–79%) | W 2 chorobach |
| NPHP1nephrocystin 1 | Często (30–79%) | W 1 chorobie |
| PLCB4phospholipase C beta 4 | Często (30–79%) | W 2 chorobach |
| PUS7pseudouridine synthase 7 | Często (30–79%) | W 1 chorobie |
| RECQLRecQ like helicase | Często (30–79%) | W 1 chorobie |
| RPL10ribosomal protein L10 | Często (30–79%) | W 2 chorobach |
| SCAPERS-phase cyclin A associated protein in the ER | Często (30–79%) | W 1 chorobie |
| SCLT1sodium channel and clathrin linker 1 | Często (30–79%) | W 1 chorobie |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Często (30–79%) | W 1 chorobie |
| SELENONselenoprotein N | Często (30–79%) | W 1 chorobie |
| SETD5SET domain containing 5 | Często (30–79%) | W 1 chorobie |
| SMAD2SMAD family member 2 | Często (30–79%) | W 1 chorobie |
| SOX5SRY-box transcription factor 5 | Często (30–79%) | W 2 chorobach |
| SPECC1Lsperm antigen with calponin homology and coiled-coil domains 1 like | Często (30–79%) | W 1 chorobie |
| TPM2tropomyosin 2 | Często (30–79%) | W 1 chorobie |
| TPM3tropomyosin 3 | Często (30–79%) | W 1 chorobie |
| TRIM32tripartite motif containing 32 | Często (30–79%) | W 1 chorobie |
| TRIOtrio Rho guanine nucleotide exchange factor | Często (30–79%) | W 3 chorobach |
| TTC8tetratricopeptide repeat domain 8 | Często (30–79%) | W 1 chorobie |
| WDPCPWD repeat containing planar cell polarity effector | Często (30–79%) | W 1 chorobie |
| ZBTB7Azinc finger and BTB domain containing 7A | Często (30–79%) | W 1 chorobie |
| ADAMTS2ADAM metallopeptidase with thrombospondin type 1 motif 2 | Czasami (5–29%) | W 1 chorobie |
| ADAMTSL2ADAMTS like 2 | Czasami (5–29%) | W 1 chorobie |
| ASXL3ASXL transcriptional regulator 3 | Czasami (5–29%) | W 2 chorobach |
| ATXN7L3ataxin 7 like 3 | Czasami (5–29%) | W 1 chorobie |
| CAMK2Bcalcium/calmodulin dependent protein kinase II beta | Czasami (5–29%) | W 1 chorobie |
| CEP295centrosomal protein 295 | Czasami (5–29%) | W 1 chorobie |
| COL5A1collagen type V alpha 1 chain | Czasami (5–29%) | W 1 chorobie |
| DDR2discoidin domain receptor tyrosine kinase 2 | Czasami (5–29%) | W 1 chorobie |
| EDNRAendothelin receptor type A | Czasami (5–29%) | W 1 chorobie |
| FBN1fibrillin 1 | Czasami (5–29%) | W 1 chorobie |
| FBXO22F-box protein 22 | Czasami (5–29%) | W 1 chorobie |
| GRB10growth factor receptor bound protein 10 | Czasami (5–29%) | W 1 chorobie |
| HIVEP2HIVEP zinc finger 2 | Czasami (5–29%) | W 1 chorobie |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Czasami (5–29%) | W 1 chorobie |
| KIF15kinesin family member 15 | Czasami (5–29%) | W 1 chorobie |
| LOXlysyl oxidase | Czasami (5–29%) | W 1 chorobie |
| MADDMAP kinase activating death domain | Czasami (5–29%) | W 1 chorobie |
| MGAT2alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Czasami (5–29%) | W 1 chorobie |
| NEDD4LNEDD4 like E3 ubiquitin protein ligase | Czasami (5–29%) | W 1 chorobie |
| NKX6-2NK6 homeobox 2 | Czasami (5–29%) | W 1 chorobie |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Czasami (5–29%) | W 1 chorobie |
| PRMT7protein arginine methyltransferase 7 | Czasami (5–29%) | W 1 chorobie |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Czasami (5–29%) | W 1 chorobie |
| RAP1BRAP1B, member of RAS oncogene family | Czasami (5–29%) | W 1 chorobie |
| RPS6KA3ribosomal protein S6 kinase A3 | Czasami (5–29%) | W 1 chorobie |
| SCARF2scavenger receptor class F member 2 | Czasami (5–29%) | W 2 chorobach |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Czasami (5–29%) | W 2 chorobach |
| SETSET nuclear proto-oncogene | Czasami (5–29%) | W 1 chorobie |
| SETBP1SET binding protein 1 | Czasami (5–29%) | W 1 chorobie |
| SNX14sorting nexin 14 | Czasami (5–29%) | W 2 chorobach |
| SPENspen family transcriptional repressor | Czasami (5–29%) | W 1 chorobie |
| UPF3BUPF3B regulator of nonsense mediated mRNA decay | Czasami (5–29%) | W 1 chorobie |
| WBP4WW domain binding protein 4 | Czasami (5–29%) | W 1 chorobie |
| ZDHHC9zDHHC palmitoyltransferase 9 | Czasami (5–29%) | W 1 chorobie |
| ZEB2zinc finger E-box binding homeobox 2 | Czasami (5–29%) | W 2 chorobach |
| ZFXzinc finger protein X-linked | Czasami (5–29%) | W 1 chorobie |
| ZMPSTE24zinc metallopeptidase STE24 | Czasami (5–29%) | W 2 chorobach |
| AMER1APC membrane recruitment protein 1 | Nie odnotowano | W 1 chorobie |
| AMMECR1AMMECR nuclear protein 1 | Nie odnotowano | W 1 chorobie |
| ATRATR checkpoint kinase | Nie odnotowano | W 1 chorobie |
| BCORBCL6 corepressor | Nie odnotowano | W 1 chorobie |
| C12orf57chromosome 12 open reading frame 57 | Nie odnotowano | W 1 chorobie |
| CCDC28Bcoiled-coil domain containing 28B | Nie odnotowano | W 1 chorobie |
| CCDC47coiled-coil domain containing 47 | Nie odnotowano | W 1 chorobie |
| COL3A1collagen type III alpha 1 chain | Nie odnotowano | W 1 chorobie |
| DHCR77-dehydrocholesterol reductase | Nie odnotowano | W 1 chorobie |
| DVL1dishevelled segment polarity protein 1 | Nie odnotowano | W 2 chorobach |
| FGFR1fibroblast growth factor receptor 1 | Nie odnotowano | W 1 chorobie |
| FLCNfolliculin | Nie odnotowano | W 1 chorobie |
| GJA1gap junction protein alpha 1 | Nie odnotowano | W 1 chorobie |
| IL1RAPL1interleukin 1 receptor accessory protein like 1 | Nie odnotowano | W 1 chorobie |
| MASP1MBL associated serine protease 1 | Nie odnotowano | W 1 chorobie |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Nie odnotowano | W 1 chorobie |
| PCGF2polycomb group ring finger 2 | Nie odnotowano | W 1 chorobie |
| PEX6peroxisomal biogenesis factor 6 | Nie odnotowano | W 1 chorobie |
| PIGKphosphatidylinositol glycan anchor biosynthesis class K | Nie odnotowano | W 1 chorobie |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Nie odnotowano | W 1 chorobie |
| RAI1retinoic acid induced 1 | Nie odnotowano | W 1 chorobie |
| ROR2ROR family WNT receptor 2 | Nie odnotowano | W 1 chorobie |
| TAF6TATA-box binding protein associated factor 6 | Nie odnotowano | W 1 chorobie |
| TRIM37tripartite motif containing 37 | Nie odnotowano | W 1 chorobie |
| TRPS1transcriptional repressor GATA binding 1 | Nie odnotowano | W 1 chorobie |
| WNT5AWnt family member 5A | Nie odnotowano | W 1 chorobie |
| XYLT1xylosyltransferase 1 | Nie odnotowano | 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 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.
AtlasKomu pomagamyNasza naukaProduktyWyniki
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