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Træk
Decreased number of teeth
Klinisk navn: Tooth agenesis
The absence of one or more teeth from the normal series by a failure to develop
Resumé
- Også kaldet
- Decreased tooth count, Fewer teeth than normal, Missing some teeth, Reduced number of teeth, Dental agenesis, Failure of development of some teeth, Teeth, agenesis
- Kropssystem
- Abnormality of head or neck
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Denne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/tooth-agenesis.json"
page <- fromJSON(url)
page$trait$nameDecreased number of teethHP:0009804
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Læs de gener, der er knyttet til Decreased number of teeth, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test44 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.
- Hypogonadotropic HypogonadismReads 15 of these genesFGFR1ANOS1CHD7FEZF1FGF17FGF8About this report →
- Treacher Collins SyndromeReads 4 of these genesPOLR1BPOLR1CPOLR1DTCOF1About this report →
- Rothmund-Thomson SyndromeReads 2 of these genesANAPC1RECQL4About this report →
- Au-Kline SyndromeReads 1 of these genesHNRNPKAbout this report →
Show 40 more reports
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- Blepharocheilodontic Syndrome 2 (CTNND1)Reads 1 of these genesCTNND1About this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- DCC-Related Mirror Movements and Agenesis of the Corpus CallosumReads 1 of these genesDCCAbout this report →
- FAT4-Related Neurodevelopmental DisorderReads 1 of these genesFAT4About this report →
- Focal Dermal Hypoplasia (Goltz Syndrome)Reads 1 of these genesPORCNAbout this report →
- Microcephalic Osteodysplastic Primordial Dwarfism Type IIReads 1 of these genesPCNTAbout this report →
- POLR1C-Related DisorderReads 1 of these genesPOLR1CAbout this report →
- Primary Microcephaly 26 (LMNB1)Reads 1 of these genesLMNB1About this report →
- SLC10A7-Related Skeletal Dysplasia With Amelogenesis ImperfectaReads 1 of these genesSLC10A7About this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- Hypodontia and AnodontiaReads 2 of these genesEDAWNT10AAbout this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 3 of these genesADAMTS3CCBE1FAT4About this report →
- Ectodermal DysplasiasReads 3 of these genesTP63EDAWNT10AAbout this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesAKT1About this report →
- Dent Disease and Lowe SyndromeReads 1 of these genesOCRLAbout this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A24About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 4 of these genesDSPCTSCGJA1WNT10AAbout this report →
- Syndromic CraniosynostosisReads 3 of these genesFGFR1FGFR2RECQL4About this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesLMNB1About this report →
- Autosomal Recessive Primary MicrocephalyReads 2 of these genesCEP152CPAPAbout this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesGHRAbout this report →
- Waardenburg SyndromeReads 1 of these genesSOX10About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesCOL9A2About this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesDSPAbout this report →
- Amelogenesis ImperfectaReads 1 of these genesFAM20AAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesDHX37About this report →
- Epidermolysis BullosaReads 1 of these genesDSPAbout this report →
- Other Inherited LeukodystrophiesReads 2 of these genesLMNB1POLR1CAbout this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesALMS1About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR1CAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesHESX1About this report →
- VitreoretinopathyReads 1 of these genesCOL9A2About this report →
- Nephrotic SyndromeReads 1 of these genesNUP85About this report →
- Osteogenesis ImperfectaReads 1 of these genesCREB3L1About this report →
- Female InfertilityReads 1 of these genesTP63About this report →
- Intellectual DisabilityReads 2 of these genesVPS13BWDR11About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesDHX37About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesLMNB1POLR1CAbout this report →
- Primary Mitochondrial DiseaseReads 1 of these genesDNA2About this report →
Læs de gener, der er knyttet til Decreased number of teeth, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test74 gener knyttet til Decreased number of teeth
Ændringer i disse gener forårsager sjældne tilstande, hvor Decreased number of teeth ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| CREB3L1cAMP responsive element binding protein 3 like 1 | Altid | I 1 tilstand |
| CTNND1catenin delta 1 | Altid | I 1 tilstand |
| DSPdesmoplakin | Altid | I 2 tilstande |
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Meget ofte (80–99 %) | I 1 tilstand |
| CCBE1collagen and calcium binding EGF domains 1 | Meget ofte (80–99 %) | I 1 tilstand |
| CTSCcathepsin C | Meget ofte (80–99 %) | I 1 tilstand |
| DPP6dipeptidyl peptidase like 6 | Meget ofte (80–99 %) | I 1 tilstand |
| FAT4FAT atypical cadherin 4 | Meget ofte (80–99 %) | I 1 tilstand |
| FGFR1fibroblast growth factor receptor 1 | Meget ofte (80–99 %) | I 3 tilstande |
| FGFR2fibroblast growth factor receptor 2 | Meget ofte (80–99 %) | I 1 tilstand |
| GHRgrowth hormone receptor | Meget ofte (80–99 %) | I 1 tilstand |
| GJA1gap junction protein alpha 1 | Meget ofte (80–99 %) | I 1 tilstand |
| LMNB1lamin B1 | Meget ofte (80–99 %) | I 1 tilstand |
| PCNTpericentrin | Meget ofte (80–99 %) | I 2 tilstande |
| SLC25A24solute carrier family 25 member 24 | Meget ofte (80–99 %) | I 1 tilstand |
| TP63tumor protein p63 | Meget ofte (80–99 %) | I 1 tilstand |
| VPS13Bvacuolar protein sorting 13 homolog B | Meget ofte (80–99 %) | I 1 tilstand |
| ATRATR checkpoint kinase | Ofte (30–79 %) | I 1 tilstand |
| ATRIPATR interacting protein | Ofte (30–79 %) | I 1 tilstand |
| CENPEcentromere protein E | Ofte (30–79 %) | I 1 tilstand |
| CEP152centrosomal protein 152 | Ofte (30–79 %) | I 1 tilstand |
| CEP295centrosomal protein 295 | Ofte (30–79 %) | I 1 tilstand |
| CEP63centrosomal protein 63 | Ofte (30–79 %) | I 1 tilstand |
| CPAPcentrosome assembly and centriole elongation protein | Ofte (30–79 %) | I 1 tilstand |
| DNA2DNA replication helicase/nuclease 2 | Ofte (30–79 %) | I 1 tilstand |
| NINninein | Ofte (30–79 %) | I 1 tilstand |
| NSMCE2NSE2 SUMO ligase component of SMC5/6 complex | Ofte (30–79 %) | I 1 tilstand |
| NUP85nucleoporin 85 | Ofte (30–79 %) | I 1 tilstand |
| PLK4polo like kinase 4 | Ofte (30–79 %) | I 1 tilstand |
| POLR1BRNA polymerase I subunit B | Ofte (30–79 %) | I 1 tilstand |
| POLR1CRNA polymerase I and III subunit C | Ofte (30–79 %) | I 1 tilstand |
| POLR1DRNA polymerase I and III subunit D | Ofte (30–79 %) | I 1 tilstand |
| PORCNporcupine O-acyltransferase | Ofte (30–79 %) | I 1 tilstand |
| RBBP8RB binding protein 8, endonuclease | Ofte (30–79 %) | I 1 tilstand |
| ROR2ROR family WNT receptor 2 | Ofte (30–79 %) | I 1 tilstand |
| TCOF1treacle ribosome biogenesis factor 1 | Ofte (30–79 %) | I 1 tilstand |
| TFAP2Atranscription factor AP-2 alpha | Ofte (30–79 %) | I 1 tilstand |
| TRAIPTRAF interacting protein | Ofte (30–79 %) | I 1 tilstand |
| AKT1AKT serine/threonine kinase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ALMS1ALMS1 centrosome and basal body associated protein | Nogle gange (5–29 %) | I 1 tilstand |
Vis 34 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| ANAPC1anaphase promoting complex subunit 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ANOS1anosmin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CCDC141coiled-coil domain containing 141 | Nogle gange (5–29 %) | I 1 tilstand |
| CHD7chromodomain helicase DNA binding protein 7 | Nogle gange (5–29 %) | I 1 tilstand |
| COL9A2collagen type IX alpha 2 chain | Nogle gange (5–29 %) | I 1 tilstand |
| DCCDCC netrin 1 receptor | Nogle gange (5–29 %) | I 1 tilstand |
| DHCR77-dehydrocholesterol reductase | Nogle gange (5–29 %) | I 1 tilstand |
| DHX37DEAH-box helicase 37 | Nogle gange (5–29 %) | I 1 tilstand |
| DUSP6dual specificity phosphatase 6 | Nogle gange (5–29 %) | I 1 tilstand |
| EMX2empty spiracles homeobox 2 | Nogle gange (5–29 %) | I 1 tilstand |
| FAM20AFAM20A golgi associated secretory pathway pseudokinase | Nogle gange (5–29 %) | I 1 tilstand |
| FEZF1FEZ family zinc finger 1 | Nogle gange (5–29 %) | I 1 tilstand |
| FGF17fibroblast growth factor 17 | Nogle gange (5–29 %) | I 1 tilstand |
| FGF8fibroblast growth factor 8 | Nogle gange (5–29 %) | I 1 tilstand |
| FLRT3fibronectin leucine rich transmembrane protein 3 | Nogle gange (5–29 %) | I 1 tilstand |
| HESX1HESX homeobox 1 | Nogle gange (5–29 %) | I 1 tilstand |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Nogle gange (5–29 %) | I 2 tilstande |
| HS6ST1heparan sulfate 6-O-sulfotransferase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| IL17RDinterleukin 17 receptor D | Nogle gange (5–29 %) | I 1 tilstand |
| NDNFneuron derived neurotrophic factor | Nogle gange (5–29 %) | I 1 tilstand |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Nogle gange (5–29 %) | I 1 tilstand |
| PLXND1plexin D1 | Nogle gange (5–29 %) | I 1 tilstand |
| PROK2prokineticin 2 | Nogle gange (5–29 %) | I 1 tilstand |
| PROKR2prokineticin receptor 2 | Nogle gange (5–29 %) | I 1 tilstand |
| RECQL4RecQ like helicase 4 | Nogle gange (5–29 %) | I 1 tilstand |
| REV3LREV3 like, DNA directed polymerase zeta catalytic subunit | Nogle gange (5–29 %) | I 1 tilstand |
| SEMA3Asemaphorin 3A | Nogle gange (5–29 %) | I 1 tilstand |
| SOX10SRY-box transcription factor 10 | Nogle gange (5–29 %) | I 1 tilstand |
| SPRY4sprouty RTK signaling antagonist 4 | Nogle gange (5–29 %) | I 1 tilstand |
| TACR3tachykinin receptor 3 | Nogle gange (5–29 %) | I 1 tilstand |
| WDR11WD repeat domain 11 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC10A7solute carrier family 10 member 7 | Sjældent (1–4%) | I 1 tilstand |
| EDAectodysplasin A | Ikke registreret | I 1 tilstand |
| WNT10AWnt family member 10A | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
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Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
AtlasHvem vi hjælperVores videnskabProdukterResultater
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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.
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