AtlasEgenskap
Progressive degeneration of movement
Klinisk navn: Motor deterioration
Loss of previously present motor (i.e., movement) abilities.
Sammendrag
- Kroppssystem
- Abnormality of the nervous system
AtlasDenne 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/motor-deterioration.json"
page <- fromJSON(url)
page$trait$nameLes genene knyttet til Progressive degeneration of movement, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test23 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.
- Megalencephalic Leukoencephalopathy with Subcortical CystsReads 3 of these genesGPRC5BHEPACAMMLC1About this report →
- Krabbe DiseaseReads 1 of these genesGALCAbout this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 3 of these genesSDHASDHBSDHDAbout this report →
Show 19 more reports
- Neuronal Ceroid LipofuscinosisReads 3 of these genesCLN8CLN5CLN6About this report →
- Lysosomal Storage DiseaseReads 6 of these genesPSAPCLN8HGSNATCLN5CLN6GALCAbout this report →
- Malignant Endocrine NeoplasmReads 2 of these genesSDHASDHBAbout this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Metachromatic LeukodystrophyReads 1 of these genesPSAPAbout this report →
- Urinary and Renal System TumourReads 2 of these genesSDHASDHBAbout this report →
- Other Inherited LeukodystrophiesReads 5 of these genesGPRC5BPSAPHEPACAMMLC1GALCAbout this report →
- Hereditary Gastrointestinal Stromal TumourReads 1 of these genesSDHBAbout this report →
- Mucopolysaccharidosis Type III (Sanfilippo Syndrome)Reads 1 of these genesHGSNATAbout this report →
- Inherited Neurodegenerative DisordersReads 9 of these genesGPRC5BPSAPCLN8HEPACAMMLC1SDHAAbout this report →
- Kidney CancerReads 1 of these genesSDHBAbout this report →
- Pyruvate Dehydrogenase & Pyruvate Carboxylase DeficiencyReads 1 of these genesPDHA1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesPDHA1PSAPSDHAGALCAbout this report →
- Leigh SyndromeReads 2 of these genesPDHA1SDHAAbout this report →
- Epilepsy (Full Panel)Reads 3 of these genesMECP2CLN8GRIN2AAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesRBM28About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesRBM28About this report →
- Retinitis PigmentosaReads 1 of these genesHGSNATAbout this report →
- Intellectual DisabilityReads 1 of these genesMECP2About this report →
Les genene knyttet til Progressive degeneration of movement, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test21 gener knyttet til Progressive degeneration of movement
Endringer i disse genene forårsaker sjeldne tilstander der Progressive degeneration of movement 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 |
|---|---|---|
| GPRC5BG protein-coupled receptor class C group 5 member B | Alltid | I 2 tilstander |
| MECP2methyl-CpG binding protein 2 | Alltid | I 1 tilstand |
| PDHA1pyruvate dehydrogenase E1 subunit alpha 1 | Alltid | I 1 tilstand |
| PSAPprosaposin | Alltid | I 1 tilstand |
| RBM28RNA binding motif protein 28 | Alltid | I 2 tilstander |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | Svært ofte (80–99 %) | I 1 tilstand |
| AQP4aquaporin 4 | Ofte (30–79 %) | I 1 tilstand |
| CLN8CLN8 transmembrane ER and ERGIC protein | Ofte (30–79 %) | I 1 tilstand |
| HEPACAMhepatic and glial cell adhesion molecule | Ofte (30–79 %) | I 1 tilstand |
| HGSNATheparan-alpha-glucosaminide N-acetyltransferase | Ofte (30–79 %) | I 1 tilstand |
| MLC1modulator of VRAC current 1 | Ofte (30–79 %) | I 1 tilstand |
| PLEKHG4pleckstrin homology and RhoGEF domain containing G4 | Ofte (30–79 %) | I 1 tilstand |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Ofte (30–79 %) | I 1 tilstand |
| SDHAF1succinate dehydrogenase complex assembly factor 1 | Ofte (30–79 %) | I 1 tilstand |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Ofte (30–79 %) | I 1 tilstand |
| SDHDsuccinate dehydrogenase complex subunit D | Ofte (30–79 %) | I 1 tilstand |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Noen ganger (5–29 %) | I 1 tilstand |
| NOTCH3notch receptor 3 | Noen ganger (5–29 %) | I 1 tilstand |
| CLN5CLN5 lysosomal BMP synthase | Ikke registrert | I 1 tilstand |
| CLN6CLN6 transmembrane ER protein | Ikke registrert | I 1 tilstand |
| GALCgalactosylceramidase | Ikke registrert | 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.
Bredere egenskaper
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.
AtlasFrom traits to your genome
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Gratis frakt · Resultater på 6–8 uker
