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Logi sisseKüsiSekveneeri oma genoom↗
Tunnus
Failure of development of more than six teeth
Kliiniline nimetus: Oligodontia
The absence of six or more teeth from the normal series by a failure to develop.
Kokkuvõte
- Teised nimetused
- Missing more than six teeth, Number of teeth decreased by more than six, Partial anodontia
- Kehasüsteem
- Abnormality of head or neck
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/oligodontia.json"
page <- fromJSON(url)
page$trait$nameKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Lugege välja geenid, mis on seotud Failure of development of more than six teeth-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test52 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.
- Hypodontia and AnodontiaReads 7 of these genesEDALRP6MSX1PAX9TSPEARWNT10AAbout this report →
- Ectodermal DysplasiasReads 9 of these genesEDAEDAREDARADDKREMEN1TSPEARWNT10AAbout this report →
- Kabuki SyndromeReads 2 of these genesKDM6AKMT2DAbout this report →
- Au-Kline SyndromeReads 1 of these genesHNRNPKAbout this report →
Show 48 more reports
- CherubismReads 1 of these genesSH3BP2About this report →
- Floating-Harbor SyndromeReads 1 of these genesSRCAPAbout this report →
- Focal Dermal Hypoplasia (Goltz Syndrome)Reads 1 of these genesPORCNAbout this report →
- Johanson-Blizzard SyndromeReads 1 of these genesUBR1About this report →
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- POLR3B-Related DisorderReads 1 of these genesPOLR3BAbout this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- Stankiewicz-Isidor SyndromeReads 1 of these genesPSMD12About this report →
- X-linked Autoinflammatory DiseaseReads 1 of these genesIKBKGAbout this report →
- Hereditary Orofacial CleftingReads 2 of these genesIRF6MSX1About this report →
- Dentinogenesis ImperfectaReads 1 of these genesSMOC2About this report →
- DOORS SyndromeReads 1 of these genesATP6V1B2About this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A24About this report →
- Familial Periodic ParalysisReads 1 of these genesKCNJ2About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesKIFBPAbout this report →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesIRF6About this report →
- Familial Atrial FibrillationReads 1 of these genesKCNJ2About this report →
- Short Qt SyndromeReads 1 of these genesKCNJ2About this report →
- Intellectual DisabilityReads 7 of these genesANKRD11BCL11BADNPHUWE1RPS6KA3SATB2About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 2 of these genesPOLR3APOLR3BAbout this report →
- Colorectal Cancer & PolyposisReads 1 of these genesAXIN2About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesPITX2About this report →
- Long QT SyndromeReads 1 of these genesKCNJ2About this report →
- Epilepsy (Full Panel)Reads 4 of these genesFLNAATP6V1B2PIGBPUM1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesKCNJ5About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesCCBE1About this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesCEP152About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesPOLR3APOLR3BAbout this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGBAbout this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesMAFAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesFGFR1About this report →
- Inherited IchthyosesReads 1 of these genesCLDN1About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesCHSY1SRD5A3About this report →
- VitreoretinopathyReads 1 of these genesIKBKGAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Severe Combined ImmunodeficiencyReads 1 of these genesBCL11BAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesPOLR3AAbout this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesWNT10AAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesPUM1About this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesPOLR3APOLR3BPUM1About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesFGFR1About this report →
- Female InfertilityReads 1 of these genesTP63About this report →
- Other Inborn Errors of ImmunityReads 2 of these genesBCL11BIKBKGAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesPOLR3BAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesPOLR3BAbout this report →
Lugege välja geenid, mis on seotud Failure of development of more than six teeth-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test70 geeni on seotud tunnusega Failure of development of more than six teeth
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Failure of development of more than six teeth. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| AXIN2axin 2 | Alati | Esineb 1 haiguses |
| DVL1dishevelled segment polarity protein 1 | Alati | Esineb 2 haiguses |
| EDAectodysplasin A | Alati | Esineb 2 haiguses |
| EDARectodysplasin A receptor | Alati | Esineb 1 haiguses |
| EDARADDEDAR associated via death domain | Alati | Esineb 3 haiguses |
| FGFR1fibroblast growth factor receptor 1 | Alati | Esineb 1 haiguses |
| GREM2gremlin 2, DAN family BMP antagonist | Alati | Esineb 1 haiguses |
| IRF6interferon regulatory factor 6 | Alati | Esineb 1 haiguses |
| KDM6Alysine demethylase 6A | Alati | Esineb 1 haiguses |
| KMT2Dlysine methyltransferase 2D | Alati | Esineb 1 haiguses |
| KREMEN1kringle containing transmembrane protein 1 | Alati | Esineb 1 haiguses |
| LRP6LDL receptor related protein 6 | Alati | Esineb 1 haiguses |
| LTBP3latent transforming growth factor beta binding protein 3 | Alati | Esineb 1 haiguses |
| MSX1msh homeobox 1 | Alati | Esineb 1 haiguses |
| PAX9paired box 9 | Alati | Esineb 2 haiguses |
| PITX2paired like homeodomain 2 | Alati | Esineb 1 haiguses |
| POLR3GLRNA polymerase III subunit GL | Alati | Esineb 1 haiguses |
| PTH1Rparathyroid hormone 1 receptor | Alati | Esineb 1 haiguses |
| SMOC2SPARC related modular calcium binding 2 | Alati | Esineb 1 haiguses |
| SUMO1small ubiquitin like modifier 1 | Alati | Esineb 1 haiguses |
| TGFAtransforming growth factor alpha | Alati | Esineb 1 haiguses |
| TSPEARthrombospondin type laminin G domain and EAR repeats | Alati | Esineb 1 haiguses |
| WNT10AWnt family member 10A | Alati | Esineb 1 haiguses |
| WNT10BWnt family member 10B | Alati | Esineb 1 haiguses |
| FLNAfilamin A | Väga sageli (80–99%) | Esineb 3 haiguses |
| SLC25A24solute carrier family 25 member 24 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ANKRD11ankyrin repeat domain 11 | Sageli (30–79%) | Esineb 2 haiguses |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Sageli (30–79%) | Esineb 1 haiguses |
| BCL11BBCL11 transcription factor B | Sageli (30–79%) | Esineb 1 haiguses |
| BCORBCL6 corepressor | Sageli (30–79%) | Esineb 2 haiguses |
| CLDN1claudin 1 | Sageli (30–79%) | Esineb 2 haiguses |
| LEF1lymphoid enhancer binding factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MAFMAF bZIP transcription factor | Sageli (30–79%) | Esineb 1 haiguses |
| PIK3C2Aphosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | Sageli (30–79%) | Esineb 2 haiguses |
| POLR3ARNA polymerase III subunit A | Sageli (30–79%) | Esineb 2 haiguses |
| POLR3BRNA polymerase III subunit B | Sageli (30–79%) | Esineb 2 haiguses |
| RMP64ribonuclease MRP subunit p64 | Sageli (30–79%) | Esineb 1 haiguses |
| SH3BP2SH3 domain binding protein 2 | Sageli (30–79%) | Esineb 2 haiguses |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ADNPactivity dependent neuroprotector homeobox | Mõnikord (5–29%) | Esineb 1 haiguses |
Näita veel 30 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| CEP152centrosomal protein 152 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CHSY1chondroitin sulfate synthase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CUX1cut like homeobox 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DVL3dishevelled segment polarity protein 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FZD2frizzled class receptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HUWE1HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KIFBPkinesin family binding protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIGBphosphatidylinositol glycan anchor biosynthesis class B | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPP1R15Bprotein phosphatase 1 regulatory subunit 15B | Mõnikord (5–29%) | Esineb 2 haiguses |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTHLHparathyroid hormone like hormone | Mõnikord (5–29%) | Esineb 1 haiguses |
| PUM1pumilio RNA binding family member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RHOAras homolog family member A | Mõnikord (5–29%) | Esineb 1 haiguses |
| RPS6KA3ribosomal protein S6 kinase A3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SATB2SATB homeobox 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SCUBE3signal peptide, CUB domain and EGF like domain containing 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SRCAPSnf2 related CREBBP activator protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRIOtrio Rho guanine nucleotide exchange factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRMT10AtRNA methyltransferase 10A | Mõnikord (5–29%) | Esineb 1 haiguses |
| WNT5AWnt family member 5A | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZRSR2zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PORCNporcupine O-acyltransferase | Harva (1–4%) | Esineb 2 haiguses |
| CCBE1collagen and calcium binding EGF domains 1 | Pole registreeritud | Esineb 1 haiguses |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Pole registreeritud | Esineb 1 haiguses |
| SRD5A3steroid 5 alpha-reductase 3 | Pole registreeritud | Esineb 1 haiguses |
| TP63tumor protein p63 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.19-9814e911.
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
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.
Alates 449 $
Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
