Træk
Truncal titubation
Tremor of the trunk in an anterior-posterior plane at 3-4 Hz.
Resumé
- Kropssystem
- Abnormality of the nervous system
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library(jsonlite)
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page$trait$nameLæs de gener, der er knyttet til Truncal titubation, og resten af dit genom, med én test.
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Bestil min Genome Test15 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.
- ACBD5 DeficiencyReads 1 of these genesACBD5About this report →
- BRAT1-Related Neurodevelopmental Disorder with Cerebellar AtrophyReads 1 of these genesBRAT1About this report →
- Thiamine Transporter and Metabolism DisordersReads 1 of these genesSLC19A3About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 3 of these genesTPP1FLVCR1THG1LAbout this report →
Show 11 more reports
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesITPR1About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesTPP1About this report →
- Inherited Neurodegenerative DisordersReads 5 of these genesTPP1HYCC1ITPR1FLVCR1THG1LAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesHYCC1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesITPR1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesTPP1About this report →
- Leigh SyndromeReads 1 of these genesSLC19A3About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesHYCC1About this report →
- Retinitis PigmentosaReads 1 of these genesFLVCR1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesBRAT1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesSLC19A3About this report →
Læs de gener, der er knyttet til Truncal titubation, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test8 gener knyttet til Truncal titubation
Ændringer i disse gener forårsager sjældne tilstande, hvor Truncal titubation 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 |
|---|---|---|
| ACBD5acyl-CoA binding domain containing 5 | Altid | I 1 tilstand |
| TPP1tripeptidyl peptidase 1 | Altid | I 1 tilstand |
| HYCC1hyccin PI4KA lipid kinase complex subunit 1 | Meget ofte (80–99 %) | I 1 tilstand |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Ofte (30–79 %) | I 1 tilstand |
| FLVCR1FLVCR choline and heme transporter 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC19A3solute carrier family 19 member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| THG1LtRNA-histidine guanylyltransferase 1 like | Nogle gange (5–29 %) | I 1 tilstand |
| BRAT1BRCA1 associated ATM activator 1 | 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.
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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Gratis forsendelse · Resultater på 6–8 uger
