Požymis
Frontotemporal dementia
A dementia associated with degeneration of the frontotemporal lobe and clinically associated with personality and behavioral changes such as disinhibition, apathy, and lack of insight. The hallmark feature of frontotemporal dementia is the presentation with focal syndromes such as progressive language dysfunction, or aphasia, or behavioral changes characteristic of frontal lobe disorders.
Santrauka
- Kūno sistema
- Abnormality of the nervous system
Share this page
Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/frontotemporal-dementia.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Frontotemporal dementia, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test25 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.
- Amyotrophic Lateral Sclerosis (ALS)Reads 23 of these genesCHCHD10CHMP2BFUSSQSTM1TARDBPTBK1About this report →
- Frontotemporal DementiaReads 13 of these genesCHCHD10CHMP2BGRNMAPTPSEN1SQSTM1About this report →
- Inherited Neurodegenerative DisordersReads 32 of these genesCHCHD10CHMP2BFUSGRNMAPTPSEN1About this report →
- Distal MyopathiesReads 6 of these genesVCPHNRNPA1HNRNPA2B1TIA1LRP12MATR3About this report →
Show 21 more report
- Amyotrophic Lateral Sclerosis Susceptibility 24 (NEK1)Reads 1 of these genesNEK1About this report →
- CYLD Cutaneous SyndromeReads 1 of these genesCYLDAbout this report →
- OPTN-Related Normal-Tension GlaucomaReads 1 of these genesOPTNAbout this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- Alzheimer diseaseReads 2 of these genesPSEN1TREM2About this report →
- Parkinson DiseaseReads 2 of these genesMAPTPLA2G6About this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesTREM2About this report →
- Familial Paget Disease of BoneReads 1 of these genesSQSTM1About this report →
- Charcot-Marie-Tooth DiseaseReads 4 of these genesVCPDCTN1FIG4NEFHAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 6 of these genesCHCHD10VCPPLA2G6DCTN1FIG4NEFHAbout this report →
- Spinal Muscular AtrophyReads 2 of these genesCHCHD10DCTN1About this report →
- GlaucomaReads 1 of these genesOPTNAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesPLA2G6About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesGRNAbout this report →
- Other Inherited LeukodystrophiesReads 2 of these genesTMEM106BTREM2About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesTMEM106BAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesATXN2About this report →
- Female InfertilityReads 1 of these genesTUBA4AAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesGRNAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesZFYVE26About this report →
- Intellectual DisabilityReads 1 of these genesERBB4About this report →
Vienu tyrimu sužinokite genus, susijusius su Frontotemporal dementia, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test44 genų susiję su Frontotemporal dementia
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Frontotemporal dementia. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Visada | 3 ligose |
| CHMP2Bcharged multivesicular body protein 2B | Labai dažnai (80–99%) | 4 ligose |
| FUSFUS RNA binding protein | Labai dažnai (80–99%) | 2 ligose |
| GRNgranulin precursor | Labai dažnai (80–99%) | 3 ligose |
| MAPTmicrotubule associated protein tau | Labai dažnai (80–99%) | 4 ligose |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | Labai dažnai (80–99%) | 1 ligoje |
| PSEN1presenilin 1 | Labai dažnai (80–99%) | 4 ligose |
| SQSTM1sequestosome 1 | Labai dažnai (80–99%) | 4 ligose |
| TARDBPTAR DNA binding protein | Labai dažnai (80–99%) | 3 ligose |
| TBK1TANK binding kinase 1 | Labai dažnai (80–99%) | 3 ligose |
| TMEM106Btransmembrane protein 106B | Labai dažnai (80–99%) | 2 ligose |
| TREM2triggering receptor expressed on myeloid cells 2 | Labai dažnai (80–99%) | 3 ligose |
| VCPvalosin containing protein | Labai dažnai (80–99%) | 6 ligose |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Dažnai (30–79%) | 2 ligose |
| HNRNPA2B1heterogeneous nuclear ribonucleoprotein A2/B1 | Dažnai (30–79%) | 2 ligose |
| PLA2G6phospholipase A2 group VI | Dažnai (30–79%) | 2 ligose |
| TIA1TIA1 cytotoxic granule associated RNA binding protein | Dažnai (30–79%) | 1 ligoje |
| ANGangiogenin | Kartais (5–29%) | 1 ligoje |
| ANXA11annexin A11 | Kartais (5–29%) | 1 ligoje |
| ATXN2ataxin 2 | Kartais (5–29%) | 1 ligoje |
| CCNFcyclin F | Kartais (5–29%) | 2 ligose |
| CFAP410cilia and flagella associated protein 410 | Kartais (5–29%) | 1 ligoje |
| DAOD-amino acid oxidase | Kartais (5–29%) | 1 ligoje |
| DCTN1dynactin subunit 1 | Kartais (5–29%) | 2 ligose |
| ERBB4erb-b2 receptor tyrosine kinase 4 | Kartais (5–29%) | 1 ligoje |
| FIG4FIG4 phosphoinositide 5-phosphatase | Kartais (5–29%) | 1 ligoje |
| GLE1GLE1 RNA export mediator | Kartais (5–29%) | 1 ligoje |
| GLT8D1glycosyltransferase 8 domain containing 1 | Kartais (5–29%) | 1 ligoje |
| LRP12LDL receptor related protein 12 | Kartais (5–29%) | 1 ligoje |
| MATR3matrin 3 | Kartais (5–29%) | 1 ligoje |
| NEFHneurofilament heavy chain | Kartais (5–29%) | 1 ligoje |
| NEK1NIMA related kinase 1 | Kartais (5–29%) | 1 ligoje |
| OPTNoptineurin | Kartais (5–29%) | 1 ligoje |
| PFN1profilin 1 | Kartais (5–29%) | 1 ligoje |
| PRPHperipherin | Kartais (5–29%) | 1 ligoje |
| SOD1superoxide dismutase 1 | Kartais (5–29%) | 1 ligoje |
| TAF15TATA-box binding protein associated factor 15 | Kartais (5–29%) | 1 ligoje |
| TUBA4Atubulin alpha 4a | Kartais (5–29%) | 1 ligoje |
| UBQLN2ubiquilin 2 | Kartais (5–29%) | 2 ligose |
| UNC13Aunc-13 homolog A | Kartais (5–29%) | 1 ligoje |
Rodyti dar 4 genų
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
Siauresni požymiai
Platesni požymiai
Iš kur tai žinoma
- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.19-9814e911.
From traits to your genome
Read the genes behind these traits in your own DNA.
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.
Nemokamas pristatymas · Rezultatai per 6–8 savaites
