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Cecha
Failure of development of more than six teeth
Nazwa kliniczna: Oligodontia
The absence of six or more teeth from the normal series by a failure to develop.
Podsumowanie
- Znana także jako
- Missing more than six teeth, Number of teeth decreased by more than six, Partial anodontia
- Układ organizmu
- Abnormality of head or neck
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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/oligodontia.json"
page <- fromJSON(url)
page$trait$nameKomu pomagamyNasza naukaProduktyWyniki
Zaloguj sięZapytajZsekwencjonuj swój genom↗
Odczytaj geny powiązane z Failure of development of more than six teeth oraz resztę swojego genomu za pomocą jednego badania.
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Zamawiam 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 →
Odczytaj geny powiązane z Failure of development of more than six teeth oraz resztę swojego genomu za pomocą jednego badania.
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Zamawiam Genome Test70 genów powiązanych z Failure of development of more than six teeth
Zmiany w tych genach powodują rzadkie choroby, w których występuje Failure of development of more than six teeth. 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 |
|---|---|---|
| AXIN2axin 2 | Zawsze | W 1 chorobie |
| DVL1dishevelled segment polarity protein 1 | Zawsze | W 2 chorobach |
| EDAectodysplasin A | Zawsze | W 2 chorobach |
| EDARectodysplasin A receptor | Zawsze | W 1 chorobie |
| EDARADDEDAR associated via death domain | Zawsze | W 3 chorobach |
| FGFR1fibroblast growth factor receptor 1 | Zawsze | W 1 chorobie |
| GREM2gremlin 2, DAN family BMP antagonist | Zawsze | W 1 chorobie |
| IRF6interferon regulatory factor 6 | Zawsze | W 1 chorobie |
| KDM6Alysine demethylase 6A | Zawsze | W 1 chorobie |
| KMT2Dlysine methyltransferase 2D | Zawsze | W 1 chorobie |
| KREMEN1kringle containing transmembrane protein 1 | Zawsze | W 1 chorobie |
| LRP6LDL receptor related protein 6 | Zawsze | W 1 chorobie |
| LTBP3latent transforming growth factor beta binding protein 3 | Zawsze | W 1 chorobie |
| MSX1msh homeobox 1 | Zawsze | W 1 chorobie |
| PAX9paired box 9 | Zawsze | W 2 chorobach |
| PITX2paired like homeodomain 2 | Zawsze | W 1 chorobie |
| POLR3GLRNA polymerase III subunit GL | Zawsze | W 1 chorobie |
| PTH1Rparathyroid hormone 1 receptor | Zawsze | W 1 chorobie |
| SMOC2SPARC related modular calcium binding 2 | Zawsze | W 1 chorobie |
| SUMO1small ubiquitin like modifier 1 | Zawsze | W 1 chorobie |
| TGFAtransforming growth factor alpha | Zawsze | W 1 chorobie |
| TSPEARthrombospondin type laminin G domain and EAR repeats | Zawsze | W 1 chorobie |
| WNT10AWnt family member 10A | Zawsze | W 1 chorobie |
| WNT10BWnt family member 10B | Zawsze | W 1 chorobie |
| FLNAfilamin A | Bardzo często (80–99%) | W 3 chorobach |
| SLC25A24solute carrier family 25 member 24 | Bardzo często (80–99%) | W 2 chorobach |
| ANKRD11ankyrin repeat domain 11 | Często (30–79%) | W 2 chorobach |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Często (30–79%) | W 1 chorobie |
| BCL11BBCL11 transcription factor B | Często (30–79%) | W 1 chorobie |
| BCORBCL6 corepressor | Często (30–79%) | W 2 chorobach |
| CLDN1claudin 1 | Często (30–79%) | W 2 chorobach |
| LEF1lymphoid enhancer binding factor 1 | Często (30–79%) | W 1 chorobie |
| MAFMAF bZIP transcription factor | Często (30–79%) | W 1 chorobie |
| PIK3C2Aphosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | Często (30–79%) | W 2 chorobach |
| POLR3ARNA polymerase III subunit A | Często (30–79%) | W 2 chorobach |
| POLR3BRNA polymerase III subunit B | Często (30–79%) | W 2 chorobach |
| RMP64ribonuclease MRP subunit p64 | Często (30–79%) | W 1 chorobie |
| SH3BP2SH3 domain binding protein 2 | Często (30–79%) | W 2 chorobach |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Często (30–79%) | W 1 chorobie |
| ADNPactivity dependent neuroprotector homeobox | Czasami (5–29%) | W 1 chorobie |
Pokaż jeszcze 30 genów
| Gen | Jak często występuje | Choroby |
|---|---|---|
| CEP152centrosomal protein 152 | Czasami (5–29%) | W 1 chorobie |
| CHSY1chondroitin sulfate synthase 1 | Czasami (5–29%) | W 1 chorobie |
| CUX1cut like homeobox 1 | Czasami (5–29%) | W 1 chorobie |
| DVL3dishevelled segment polarity protein 3 | Czasami (5–29%) | W 1 chorobie |
| FZD2frizzled class receptor 2 | Czasami (5–29%) | W 1 chorobie |
| HUWE1HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1 | Czasami (5–29%) | W 1 chorobie |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Czasami (5–29%) | W 1 chorobie |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Czasami (5–29%) | W 2 chorobach |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Czasami (5–29%) | W 1 chorobie |
| KIFBPkinesin family binding protein | Czasami (5–29%) | W 1 chorobie |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Czasami (5–29%) | W 1 chorobie |
| PIGBphosphatidylinositol glycan anchor biosynthesis class B | Czasami (5–29%) | W 1 chorobie |
| PPP1R15Bprotein phosphatase 1 regulatory subunit 15B | Czasami (5–29%) | W 2 chorobach |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Czasami (5–29%) | W 1 chorobie |
| PTHLHparathyroid hormone like hormone | Czasami (5–29%) | W 1 chorobie |
| PUM1pumilio RNA binding family member 1 | Czasami (5–29%) | W 1 chorobie |
| RHOAras homolog family member A | Czasami (5–29%) | W 1 chorobie |
| RPS6KA3ribosomal protein S6 kinase A3 | Czasami (5–29%) | W 2 chorobach |
| SATB2SATB homeobox 2 | Czasami (5–29%) | W 2 chorobach |
| SCUBE3signal peptide, CUB domain and EGF like domain containing 3 | Czasami (5–29%) | W 1 chorobie |
| SRCAPSnf2 related CREBBP activator protein | Czasami (5–29%) | W 1 chorobie |
| TRIOtrio Rho guanine nucleotide exchange factor | Czasami (5–29%) | W 1 chorobie |
| TRMT10AtRNA methyltransferase 10A | Czasami (5–29%) | W 1 chorobie |
| WNT5AWnt family member 5A | Czasami (5–29%) | W 1 chorobie |
| ZRSR2zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2 | Czasami (5–29%) | W 1 chorobie |
| PORCNporcupine O-acyltransferase | Rzadko (1–4%) | W 2 chorobach |
| CCBE1collagen and calcium binding EGF domains 1 | Nie odnotowano | W 1 chorobie |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Nie odnotowano | W 1 chorobie |
| SRD5A3steroid 5 alpha-reductase 3 | Nie odnotowano | W 1 chorobie |
| TP63tumor protein p63 | 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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From traits to your genome
Read the genes behind these traits in your own DNA.
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