AtlasTræk
Progressive spasticity
Spasticity that increases in degree with time.
Resumé
- Også kaldet
- Spasticity, progressive
AtlasDenne 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/progressive-spasticity.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Progressive spasticity, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test24 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.
- Acromelic Frontonasal DysostosisReads 1 of these genesZSWIM6About this report →
- Basilicata-Akhtar SyndromeReads 1 of these genesMSL3About this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- Krabbe DiseaseReads 1 of these genesGALCAbout this report →
Show 20 more reports
- OPA1-Related Optic AtrophyReads 1 of these genesOPA1About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- Other Inherited LeukodystrophiesReads 6 of these genesGALCHSPD1DARS2NKX6-2DEGS1GJC2About this report →
- Inherited Neurodegenerative DisordersReads 12 of these genesGALCHSPD1SELENOISPG11DARS2NKX6-2About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 3 of these genesHSPD1DEGS1GJC2About this report →
- Hereditary Spastic ParaplegiaReads 4 of these genesHSPD1SELENOISPG11GJC2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 6 of these genesGALCSERAC1SPG11PLA2G6POLGOPA1About this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesGLRX5About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesPLA2G6About this report →
- Hereditary Optic NeuropathyReads 1 of these genesOPA1About this report →
- Parkinson DiseaseReads 1 of these genesPLA2G6About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesGJC2About this report →
- Leigh SyndromeReads 2 of these genesSERAC1OPA1About this report →
- Intellectual DisabilityReads 3 of these genesRPS6KA3CTNNB1MECP2About this report →
- VitreoretinopathyReads 1 of these genesCTNNB1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesSPG11About this report →
- Primary Mitochondrial DiseaseReads 2 of these genesPOLGOPA1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGALCAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesSPG11About this report →
- Epilepsy (Full Panel)Reads 1 of these genesMECP2About this report →
Læs de gener, der er knyttet til Progressive spasticity, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test20 gener knyttet til Progressive spasticity
Ændringer i disse gener forårsager sjældne tilstande, hvor Progressive spasticity 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 |
|---|---|---|
| GALCgalactosylceramidase | Altid | I 1 tilstand |
| HSPD1heat shock protein family D (Hsp60) member 1 | Altid | I 1 tilstand |
| SELENOIselenoprotein I | Altid | I 1 tilstand |
| TAF8TATA-box binding protein associated factor 8 | Altid | I 1 tilstand |
| GLRX5glutaredoxin 5 | Meget ofte (80–99 %) | I 1 tilstand |
| SERAC1serine active site containing 1 | Meget ofte (80–99 %) | I 1 tilstand |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Meget ofte (80–99 %) | I 1 tilstand |
| DARS2aspartyl-tRNA synthetase 2, mitochondrial | Ofte (30–79 %) | I 1 tilstand |
| MSL3MSL complex subunit 3 | Ofte (30–79 %) | I 1 tilstand |
| NKX6-2NK6 homeobox 2 | Ofte (30–79 %) | I 1 tilstand |
| PLA2G6phospholipase A2 group VI | Ofte (30–79 %) | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Ofte (30–79 %) | I 1 tilstand |
| RPS6KA3ribosomal protein S6 kinase A3 | Ofte (30–79 %) | I 1 tilstand |
| TBCDtubulin folding cofactor D | Ofte (30–79 %) | I 1 tilstand |
| ZSWIM6zinc finger SWIM-type containing 6 | Ofte (30–79 %) | I 1 tilstand |
| CTNNB1catenin beta 1 | Nogle gange (5–29 %) | I 1 tilstand |
| DEGS1delta 4-desaturase, sphingolipid 1 | Ikke registreret | I 1 tilstand |
| GJC2gap junction protein gamma 2 | Ikke registreret | I 1 tilstand |
| MECP2methyl-CpG binding protein 2 | Ikke registreret | I 1 tilstand |
| OPA1OPA1 mitochondrial dynamin like GTPase | 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.
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 2026.10.18-8b139e39.
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