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Egenskap
Abnormality of the palate
Klinisk navn: Abnormal palate morphology
Any abnormality of the palate, i.e., of roof of the mouth.
Sammendrag
- Også kalt
- Abnormality of the roof of the mouth, Palatal anomaly, Palate abnormality
- Kroppssystem
- Abnormality of head or neck
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Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese 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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Les genene knyttet til Abnormality of the palate, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt 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 →
Les genene knyttet til Abnormality of the palate, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test48 gener knyttet til Abnormality of the palate
Endringer i disse genene forårsaker sjeldne tilstander der Abnormality of the palate forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ATP7AATPase copper transporting alpha | Svært ofte (80–99 %) | I 1 tilstand |
| COL12A1collagen type XII alpha 1 chain | Svært ofte (80–99 %) | I 1 tilstand |
| COL6A1collagen type VI alpha 1 chain | Svært ofte (80–99 %) | I 1 tilstand |
| COL6A2collagen type VI alpha 2 chain | Svært ofte (80–99 %) | I 1 tilstand |
| COL6A3collagen type VI alpha 3 chain | Svært ofte (80–99 %) | I 1 tilstand |
| PEX1peroxisomal biogenesis factor 1 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX10peroxisomal biogenesis factor 10 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX11Bperoxisomal biogenesis factor 11 beta | Svært ofte (80–99 %) | I 1 tilstand |
| PEX12peroxisomal biogenesis factor 12 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX13peroxisomal biogenesis factor 13 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX14peroxisomal biogenesis factor 14 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX16peroxisomal biogenesis factor 16 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX19peroxisomal biogenesis factor 19 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX2peroxisomal biogenesis factor 2 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX26peroxisomal biogenesis factor 26 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX3peroxisomal biogenesis factor 3 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX5peroxisomal biogenesis factor 5 | Svært ofte (80–99 %) | I 1 tilstand |
| PEX6peroxisomal biogenesis factor 6 | Svært ofte (80–99 %) | I 1 tilstand |
| RNU12RNA, U12 small nuclear | Svært ofte (80–99 %) | I 1 tilstand |
| TCF4transcription factor 4 | Svært ofte (80–99 %) | I 1 tilstand |
| ZBTB20zinc finger and BTB domain containing 20 | Svært ofte (80–99 %) | I 1 tilstand |
| ZNHIT3zinc finger HIT-type containing 3 | Svært 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 | Noen ganger (5–29 %) | I 1 tilstand |
| FGFR3fibroblast growth factor receptor 3 | Noen ganger (5–29 %) | I 1 tilstand |
| FIG4FIG4 phosphoinositide 5-phosphatase | Noen ganger (5–29 %) | I 1 tilstand |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Noen ganger (5–29 %) | I 1 tilstand |
| NLRP3NLR family pyrin domain containing 3 | Noen ganger (5–29 %) | I 1 tilstand |
| NXNnucleoredoxin | Noen ganger (5–29 %) | I 1 tilstand |
Vis 8 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| POLR1ARNA polymerase I subunit A | Noen ganger (5–29 %) | I 1 tilstand |
| PPP1CBprotein phosphatase 1 catalytic subunit beta | Noen ganger (5–29 %) | I 1 tilstand |
| RAD21RAD21 cohesin complex component | Noen ganger (5–29 %) | I 1 tilstand |
| ROR2ROR family WNT receptor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| SHOC2SHOC2 leucine rich repeat scaffold protein | Noen ganger (5–29 %) | I 1 tilstand |
| SIN3ASIN3 transcription regulator family member A | Noen ganger (5–29 %) | I 1 tilstand |
| TRPS1transcriptional repressor GATA binding 1 | Noen ganger (5–29 %) | I 1 tilstand |
| TXNL4Athioredoxin like 4A | Noen ganger (5–29 %) | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
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Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.19-9814e911.
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