Tunnus
Abnormality of dental shape
Kliiniline nimetus: Abnormal dental morphology
An abnormality of the morphology of the tooth.
Kokkuvõte
- Teised nimetused
- Abnormally shaped teeth, Deformity of teeth, Dental deformity, Dental malformations, Malformed teeth, Misshapen teeth, Misshapened teeth, Abnormality of dental morphology, Abnormality of shape of tooth, Malformation of teeth
- Kehasüsteem
- Abnormality of head or neck
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Abnormality of dental shape, and the rest of your genome, with one test.
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Telli oma Genome Test70 geeni on seotud tunnusega Abnormality of dental shape
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Abnormality of dental shape. 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 |
|---|---|---|
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ANTXR2ANTXR cell adhesion molecule 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CCBE1collagen and calcium binding EGF domains 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CDH3cadherin 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DHCR77-dehydrocholesterol reductase | Väga sageli (80–99%) | Esineb 1 haiguses |
| EDARectodysplasin A receptor | Väga sageli (80–99%) | Esineb 2 haiguses |
| EDARADDEDAR associated via death domain | Väga sageli (80–99%) | Esineb 3 haiguses |
| FAT4FAT atypical cadherin 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KDF1keratinocyte differentiation factor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LONP1lon peptidase 1, mitochondrial | Väga sageli (80–99%) | Esineb 1 haiguses |
| LRP6LDL receptor related protein 6 | Väga sageli (80–99%) | Esineb 2 haiguses |
| MSX1msh homeobox 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Väga sageli (80–99%) | Esineb 1 haiguses |
| RNU12RNA, U12 small nuclear | Väga sageli (80–99%) | Esineb 1 haiguses |
| RPS6KA3ribosomal protein S6 kinase A3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TRAF6TNF receptor associated factor 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Sageli (30–79%) | Esineb 1 haiguses |
| BCORBCL6 corepressor | Sageli (30–79%) | Esineb 1 haiguses |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Sageli (30–79%) | Esineb 1 haiguses |
| CLIP2CAP-Gly domain containing linker protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| CSTBcystatin B | Sageli (30–79%) | Esineb 1 haiguses |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Sageli (30–79%) | Esineb 1 haiguses |
| EIF4Heukaryotic translation initiation factor 4H | Sageli (30–79%) | Esineb 1 haiguses |
| ELNelastin | Sageli (30–79%) | Esineb 1 haiguses |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Sageli (30–79%) | Esineb 1 haiguses |
| GTF2Igeneral transcription factor IIi | Sageli (30–79%) | Esineb 1 haiguses |
| GTF2IRD1GTF2I repeat domain containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GTF2IRD2GTF2I repeat domain containing 2 | Sageli (30–79%) | Esineb 1 haiguses |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Sageli (30–79%) | Esineb 1 haiguses |
| KDM6Alysine demethylase 6A | Sageli (30–79%) | Esineb 1 haiguses |
| KMT2Dlysine methyltransferase 2D | Sageli (30–79%) | Esineb 1 haiguses |
| KRT14keratin 14 | Sageli (30–79%) | Esineb 1 haiguses |
| LIMK1LIM domain kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| METTL27methyltransferase like 27 | Sageli (30–79%) | Esineb 1 haiguses |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Sageli (30–79%) | Esineb 1 haiguses |
| NCF1neutrophil cytosolic factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NECTIN1nectin cell adhesion molecule 1 | Sageli (30–79%) | Esineb 1 haiguses |
| RFC2replication factor C subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SH3BP2SH3 domain binding protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| STX1Asyntaxin 1A | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 30 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| TBL2transducin beta like 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TMEM270transmembrane protein 270 | Sageli (30–79%) | Esineb 1 haiguses |
| TP63tumor protein p63 | Sageli (30–79%) | Esineb 1 haiguses |
| VPS37DVPS37D subunit of ESCRT-I | Sageli (30–79%) | Esineb 1 haiguses |
| WNT10AWnt family member 10A | Sageli (30–79%) | Esineb 2 haiguses |
| EDAectodysplasin A | Mõnikord (5–29%) | Esineb 1 haiguses |
| FGFR1fibroblast growth factor receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GREM2gremlin 2, DAN family BMP antagonist | Mõnikord (5–29%) | Esineb 1 haiguses |
| IRF6interferon regulatory factor 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PAX9paired box 9 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PKP1plakophilin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| POLR1BRNA polymerase I subunit B | Mõnikord (5–29%) | Esineb 1 haiguses |
| POLR1CRNA polymerase I and III subunit C | Mõnikord (5–29%) | Esineb 1 haiguses |
| POLR1DRNA polymerase I and III subunit D | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAI1retinoic acid induced 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SUMO1small ubiquitin like modifier 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TCOF1treacle ribosome biogenesis factor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TGFAtransforming growth factor alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| WNT10BWnt family member 10B | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZEB2zinc finger E-box binding homeobox 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| CLCN7Cl-/H+ antiporter 7 | Harva (1–4%) | Esineb 1 haiguses |
| PLEKHM1pleckstrin homology and RUN domain containing M1 | Harva (1–4%) | Esineb 1 haiguses |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Harva (1–4%) | Esineb 1 haiguses |
| ADAMTS10ADAM metallopeptidase with thrombospondin type 1 motif 10 | Pole registreeritud | Esineb 1 haiguses |
| CKAP2Lcytoskeleton associated protein 2L | Pole registreeritud | Esineb 1 haiguses |
| FBN1fibrillin 1 | Pole registreeritud | Esineb 1 haiguses |
| HRASHRas proto-oncogene, GTPase | Pole registreeritud | Esineb 1 haiguses |
| KRASKRas proto-oncogene, GTPase | Pole registreeritud | Esineb 1 haiguses |
| NRASNRAS proto-oncogene, GTPase | Pole registreeritud | Esineb 1 haiguses |
| SATB1SATB homeobox 1 | 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.
Kitsamad tunnused
- Decreased size of tooth177 geeni
- Cone shaped tooth29 geeni
- Abnormal dental position28 geeni
- Increased size of tooth21 geeni
- Abnormality of canine16 geeni
- Irregular teeth6 geeni
- Abnormality of baby teeth4 geeni
- Abnormality of tooth part2 geeni
- Fragile teeth2 geeni
- Abnormal shape of molar tooth1 geen
- Abnormality of the dental root1 geen
- Excessive wear and tear on teeth1 geen
- Abnormal number of teeth
- Abnormality of shape of incisor
- Abnormality of shape of premolar
- Double tooth
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 2026.10.16-c6eea6bf.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast