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Træk
Abnormality of the palate
Klinisk navn: Abnormal palate morphology
Any abnormality of the palate, i.e., of roof of the mouth.
Resumé
- Også kaldet
- Abnormality of the roof of the mouth, Palatal anomaly, Palate abnormality
- 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/abnormal-palate-morphology.json"
page <- fromJSON(url)
page$trait$nameAbnormality of the palateHP:0000174
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Læs de gener, der er knyttet til Abnormality of the palate, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test38 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.
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 13 of these genesPEX1PEX10PEX11BPEX12PEX13PEX14About this report →
- Other Inherited LeukodystrophiesReads 13 of these genesPEX1PEX10PEX11BPEX12PEX13PEX14About this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- Burn-McKeown SyndromeReads 1 of these genesTXNL4AAbout this report →
Show 34 more reports
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- GAPO SyndromeReads 1 of these genesANTXR1About this report →
- KDM1A-Related Neurodevelopmental DisorderReads 1 of these genesKDM1AAbout this report →
- Primrose SyndromeReads 1 of these genesZBTB20About this report →
- SF3B4-Related Acrofacial Dysostosis (Nager Syndrome)Reads 1 of these genesSF3B4About this report →
- Rare Hereditary Peripheral NeuropathiesReads 15 of these genesATP7APEX1PEX10PEX11BPEX12PEX13About this report →
- Inherited Neurodegenerative DisordersReads 17 of these genesATP7APEX1PEX10PEX11BPEX12PEX13About this report →
- Congenital Muscular DystrophiesReads 4 of these genesCOL12A1COL6A1COL6A2COL6A3About this report →
- Hereditary Multiple OsteochondromasReads 1 of these genesEXT1About this report →
- Syndromic CraniosynostosisReads 3 of these genesRNU12FGFR2FGFR3About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRMRPAbout this report →
- Limb-Girdle Muscular DystrophyReads 3 of these genesCOL6A1COL6A2COL6A3About this report →
- Noonan SyndromeReads 2 of these genesPPP1CBSHOC2About this report →
- Cornelia de Lange SyndromeReads 1 of these genesRAD21About this report →
- Hereditary Orofacial CleftingReads 1 of these genesTBX22About this report →
- Hereditary Periodic Fever SyndromesReads 1 of these genesNLRP3About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesTUBG1About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesPPP1CBSHOC2About this report →
- Cutis LaxaReads 1 of these genesATP7AAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesATP7AFIG4About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesCOL12A1About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesTUBG1About this report →
- Intellectual DisabilityReads 3 of these genesTCF4DDX3XSIN3AAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Spinal Muscular AtrophyReads 1 of these genesATP7AAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesFIG4About this report →
- Diabetes MellitusReads 1 of these genesZBTB20About this report →
- Inherited ThrombocytopeniasReads 1 of these genesFLI1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesCOL6A3About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesPEX6About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesNIPA1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesRMRPAbout this report →
Læs de gener, der er knyttet til Abnormality of the palate, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test48 gener knyttet til Abnormality of the palate
Ændringer i disse gener forårsager sjældne tilstande, hvor Abnormality of the palate 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 |
|---|---|---|
| ATP7AATPase copper transporting alpha | Meget ofte (80–99 %) | I 1 tilstand |
| COL12A1collagen type XII alpha 1 chain | Meget ofte (80–99 %) | I 1 tilstand |
| COL6A1collagen type VI alpha 1 chain | Meget ofte (80–99 %) | I 1 tilstand |
| COL6A2collagen type VI alpha 2 chain | Meget ofte (80–99 %) | I 1 tilstand |
| COL6A3collagen type VI alpha 3 chain | Meget ofte (80–99 %) | I 1 tilstand |
| PEX1peroxisomal biogenesis factor 1 | Meget ofte (80–99 %) | I 1 tilstand |
| PEX10peroxisomal biogenesis factor 10 | Meget ofte (80–99 %) | I 1 tilstand |
| PEX11Bperoxisomal biogenesis factor 11 beta | Meget ofte (80–99 %) | I 1 tilstand |
| PEX12peroxisomal biogenesis factor 12 | Meget ofte (80–99 %) | I 1 tilstand |
| PEX13peroxisomal biogenesis factor 13 | Meget ofte (80–99 %) | I 1 tilstand |
| PEX14peroxisomal biogenesis factor 14 | Meget ofte (80–99 %) | I 1 tilstand |
| PEX16peroxisomal biogenesis factor 16 | Meget ofte (80–99 %) | I 1 tilstand |
| PEX19peroxisomal biogenesis factor 19 | Meget ofte (80–99 %) | I 1 tilstand |
| PEX2peroxisomal biogenesis factor 2 | Meget ofte (80–99 %) | I 1 tilstand |
| PEX26peroxisomal biogenesis factor 26 | Meget ofte (80–99 %) | I 1 tilstand |
| PEX3peroxisomal biogenesis factor 3 | Meget ofte (80–99 %) | I 1 tilstand |
| PEX5peroxisomal biogenesis factor 5 | Meget ofte (80–99 %) | I 1 tilstand |
| PEX6peroxisomal biogenesis factor 6 | Meget ofte (80–99 %) | I 1 tilstand |
| RNU12RNA, U12 small nuclear | Meget ofte (80–99 %) | I 1 tilstand |
| TCF4transcription factor 4 | Meget ofte (80–99 %) | I 1 tilstand |
| ZBTB20zinc finger and BTB domain containing 20 | Meget ofte (80–99 %) | I 1 tilstand |
| ZNHIT3zinc finger HIT-type containing 3 | Meget ofte (80–99 %) | I 1 tilstand |
| ANTXR1ANTXR cell adhesion molecule 1 | Ofte (30–79 %) | I 1 tilstand |
| BCORBCL6 corepressor | Ofte (30–79 %) | I 1 tilstand |
| DDX3XDEAD-box helicase 3 X-linked | Ofte (30–79 %) | I 1 tilstand |
| FGFR2fibroblast growth factor receptor 2 | Ofte (30–79 %) | I 1 tilstand |
| KDM1Alysine demethylase 1A | Ofte (30–79 %) | I 1 tilstand |
| NIPA1NIPA magnesium transporter 1 | Ofte (30–79 %) | I 1 tilstand |
| NIPA2NIPA magnesium transporter 2 | Ofte (30–79 %) | I 1 tilstand |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Ofte (30–79 %) | I 1 tilstand |
| SF3B4splicing factor 3b subunit 4 | Ofte (30–79 %) | I 1 tilstand |
| TBX22T-box transcription factor 22 | Ofte (30–79 %) | I 1 tilstand |
| TRIM33tripartite motif containing 33 | Ofte (30–79 %) | I 1 tilstand |
| TUBG1tubulin gamma 1 | Ofte (30–79 %) | I 1 tilstand |
| EXT1exostosin glycosyltransferase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| FGFR3fibroblast growth factor receptor 3 | Nogle gange (5–29 %) | I 1 tilstand |
| FIG4FIG4 phosphoinositide 5-phosphatase | Nogle gange (5–29 %) | I 1 tilstand |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Nogle gange (5–29 %) | I 1 tilstand |
| NLRP3NLR family pyrin domain containing 3 | Nogle gange (5–29 %) | I 1 tilstand |
| NXNnucleoredoxin | Nogle gange (5–29 %) | I 1 tilstand |
Vis 8 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| POLR1ARNA polymerase I subunit A | Nogle gange (5–29 %) | I 1 tilstand |
| PPP1CBprotein phosphatase 1 catalytic subunit beta | Nogle gange (5–29 %) | I 1 tilstand |
| RAD21RAD21 cohesin complex component | Nogle gange (5–29 %) | I 1 tilstand |
| ROR2ROR family WNT receptor 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SHOC2SHOC2 leucine rich repeat scaffold protein | Nogle gange (5–29 %) | I 1 tilstand |
| SIN3ASIN3 transcription regulator family member A | Nogle gange (5–29 %) | I 1 tilstand |
| TRPS1transcriptional repressor GATA binding 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TXNL4Athioredoxin like 4A | Nogle gange (5–29 %) | 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.
Snævrere træk
Bredere træk
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.
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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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