AtlasTunnus
Difficulty making arithmetical calculations
Kliiniline nimetus: Dyscalculia
A specific learning disability involving mathematics and arithmetic.
Kokkuvõte
- Teised nimetused
- Acalculia
- Kehasüsteem
- Abnormality of the nervous system
AtlasSelle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/dyscalculia.json"
page <- fromJSON(url)
page$trait$nameLugege välja geenid, mis on seotud Difficulty making arithmetical calculations-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test33 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.
- Frontotemporal DementiaReads 12 of these genesCYLDCHMP2BGRNMAPTPSEN1SQSTM1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 10 of these genesCYLDCHMP2BSQSTM1VCPCHCHD10FUSAbout this report →
- CYLD Cutaneous SyndromeReads 1 of these genesCYLDAbout this report →
- Inherited Neurodegenerative DisordersReads 19 of these genesCYLDITPR1CHMP2BGRNMAPTPSEN1About this report →
Show 29 more reports
- Alzheimer diseaseReads 2 of these genesPSEN1TREM2About this report →
- Distal MyopathiesReads 3 of these genesVCPHNRNPA1HNRNPA2B1About this report →
- Familial Hemiplegic MigraineReads 1 of these genesCACNA1AAbout this report →
- 46,XX Differences of Sex DevelopmentReads 1 of these genesSRYAbout 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 →
- Hereditary Episodic AtaxiasReads 1 of these genesCACNA1AAbout this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesMAP1BAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 2 of these genesITPR1CACNA1AAbout this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesITPR1About this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesCACNA1AAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesGRNAbout this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesAPC2About this report →
- Parkinson DiseaseReads 1 of these genesMAPTAbout this report →
- Hypertrophic CardiomyopathyReads 2 of these genesNSD1SRYAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesSRYAbout this report →
- Other Inherited LeukodystrophiesReads 2 of these genesTMEM106BTREM2About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesAPC2About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesTMEM106BAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesVCPCHCHD10PNKPAbout this report →
- Spinal Muscular AtrophyReads 1 of these genesCHCHD10About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesPNKPAbout this report →
- Epilepsy (Full Panel)Reads 2 of these genesPNKPCACNA1AAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesPNKPAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesGRNAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesVCPAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesMAP1BAbout this report →
Lugege välja geenid, mis on seotud Difficulty making arithmetical calculations-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test23 geeni on seotud tunnusega Difficulty making arithmetical calculations
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Difficulty making arithmetical calculations. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| CYLDCYLD lysine 63 deubiquitinase | Alati | Esineb 1 haiguses |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Alati | Esineb 1 haiguses |
| CHMP2Bcharged multivesicular body protein 2B | Väga sageli (80–99%) | Esineb 2 haiguses |
| GRNgranulin precursor | Väga sageli (80–99%) | Esineb 1 haiguses |
| MAPTmicrotubule associated protein tau | Väga sageli (80–99%) | Esineb 1 haiguses |
| PSEN1presenilin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SQSTM1sequestosome 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TMEM106Btransmembrane protein 106B | Väga sageli (80–99%) | Esineb 1 haiguses |
| TREM2triggering receptor expressed on myeloid cells 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| VCPvalosin containing protein | Väga sageli (80–99%) | Esineb 3 haiguses |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Sageli (30–79%) | Esineb 1 haiguses |
| FUSFUS RNA binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| TARDBPTAR DNA binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| TBK1TANK binding kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| APC2APC regulator of Wnt signaling pathway 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNRNPA2B1heterogeneous nuclear ribonucleoprotein A2/B1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAP1Bmicrotubule associated protein 1B | Mõnikord (5–29%) | Esineb 1 haiguses |
| NSD1nuclear receptor binding SET domain protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PNKPpolynucleotide kinase 3'-phosphatase | Mõnikord (5–29%) | Esineb 1 haiguses |
| SRYsex determining region Y | Mõnikord (5–29%) | Esineb 1 haiguses |
| C9orf72C9orf72-SMCR8 complex subunit | Pole registreeritud | Esineb 1 haiguses |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.19-9814e911.
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Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
