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PrisijungtiKlaustiSekvenuokite savo genomą↗
Požymis
Language impairment
Language impairment is a deficit in comprehension or production of language that includes reduced vocabulary, limited sentence structure, or impairments in written or spoken communication. Language abilities are substantially and quantifiably below age expectations.
Santrauka
- Taip pat vadinama
- Language disorder
- Kūno sistema
- Abnormality of the nervous system
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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/language-impairment.json"
page <- fromJSON(url)
page$trait$nameLanguage impairmentHP:0002463
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Language impairment, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test38 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 20 of these genesANGANXA11CCNFCHCHD10CHMP2BDCTN1About this report →
- Frontotemporal DementiaReads 10 of these genesPSEN1CCNFCHCHD10CHMP2BHNRNPA1HNRNPA2B1About this report →
- Alzheimer diseaseReads 4 of these genesAPPPSEN1PSEN2TREM2About this report →
- Familial Hemiplegic MigraineReads 3 of these genesATP1A2CACNA1ASCN1AAbout this report →
Show 34 more reports
- Distal MyopathiesReads 5 of these genesHNRNPA1HNRNPA2B1LRP12MATR3VCPAbout this report →
- Birt-Hogg-Dubé SyndromeReads 1 of these genesFLCNAbout this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Charcot-Marie-Tooth DiseaseReads 6 of these genesDCTN1FIG4GJB1NEFHPRPS1VCPAbout this report →
- Epilepsy (Full Panel)Reads 9 of these genesGRIN2AATP1A2CACNA1ACPLX1PRRT2SCN1AAbout this report →
- Cerebral Amyloid AngiopathyReads 1 of these genesAPPAbout this report →
- Intellectual DisabilityReads 8 of these genesFOXP1GATAD2BEHMT1ERBB4KMT2CMBD5About 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 →
- NeurofibromatosisReads 1 of these genesNF1About this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 1 of these genesHNF1BAbout this report →
- Hereditary Orofacial CleftingReads 1 of these genesGRHL3About this report →
- Systemic Lupus ErythematosusReads 1 of these genesSAT1About this report →
- Spinal Muscular AtrophyReads 2 of these genesCHCHD10DCTN1About this report →
- GlaucomaReads 1 of these genesOPTNAbout this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesABCB7About this report →
- Purine & Pyrimidine Metabolism DisordersReads 1 of these genesPRPS1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 2 of these genesATXN2CACNA1AAbout this report →
- Kidney CancerReads 1 of these genesFLCNAbout this report →
- Hereditary AmyloidosisReads 1 of these genesAPPAbout this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesHNF1BAbout this report →
- Urinary and Renal System TumourReads 1 of these genesFLCNAbout this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesADGRG1About this report →
- Parkinson DiseaseReads 1 of these genesMAPTAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesHNF1BAbout this report →
- Autoimmune DiseaseReads 1 of these genesSAT1About this report →
- Noonan SyndromeReads 1 of these genesMAPK1About this report →
- Hearing Loss and DeafnessReads 2 of these genesPRPS1TBC1D24About this report →
- Diabetes MellitusReads 1 of these genesHNF1BAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesPRRT2About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesMAPK1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesTREM2About this report →
Vienu tyrimu sužinokite genus, susijusius su Language impairment, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test80 genų susiję su Language impairment
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Language impairment. 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 |
|---|---|---|
| ABCB7ATP binding cassette subfamily B member 7 | Visada | 1 ligoje |
| ADGRG1adhesion G protein-coupled receptor G1 | Visada | 3 ligose |
| BCKDKbranched chain keto acid dehydrogenase kinase | Visada | 1 ligoje |
| FOXP1forkhead box P1 | Visada | 1 ligoje |
| GATAD2BGATA zinc finger domain containing 2B | Visada | 1 ligoje |
| APPamyloid beta precursor protein | Labai dažnai (80–99%) | 1 ligoje |
| BCRBCR activator of RhoGEF and GTPase | Labai dažnai (80–99%) | 1 ligoje |
| CRKLCRK like proto-oncogene, adaptor protein | Labai dažnai (80–99%) | 1 ligoje |
| DCXdoublecortin | Labai dažnai (80–99%) | 1 ligoje |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Labai dažnai (80–99%) | 1 ligoje |
| MAPK1mitogen-activated protein kinase 1 | Labai dažnai (80–99%) | 1 ligoje |
| PSEN1presenilin 1 | Labai dažnai (80–99%) | 3 ligose |
| PSEN2presenilin 2 | Labai dažnai (80–99%) | 1 ligoje |
| SORL1sortilin related receptor 1 | Labai dažnai (80–99%) | 1 ligoje |
| TOMM40translocase of outer mitochondrial membrane 40 | Labai dažnai (80–99%) | 1 ligoje |
| TREM2triggering receptor expressed on myeloid cells 2 | Labai dažnai (80–99%) | 2 ligose |
| GRHL3grainyhead like transcription factor 3 | Dažnai (30–79%) | 1 ligoje |
| NF1neurofibromin 1 | Dažnai (30–79%) | 1 ligoje |
| PAFAH1B1platelet activating factor acetylhydrolase 1b regulatory subunit 1 | Dažnai (30–79%) | 1 ligoje |
| PI4KAphosphatidylinositol 4-kinase alpha | Dažnai (30–79%) | 1 ligoje |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | Dažnai (30–79%) | 1 ligoje |
| SRPX2sushi repeat containing protein X-linked 2 | Dažnai (30–79%) | 1 ligoje |
| UBBubiquitin B | Dažnai (30–79%) | 1 ligoje |
| ANGangiogenin | Kartais (5–29%) | 1 ligoje |
| ANXA11annexin A11 | Kartais (5–29%) | 1 ligoje |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Kartais (5–29%) | 1 ligoje |
| ATXN2ataxin 2 | Kartais (5–29%) | 1 ligoje |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Kartais (5–29%) | 1 ligoje |
| CCNFcyclin F | Kartais (5–29%) | 1 ligoje |
| CFAP410cilia and flagella associated protein 410 | Kartais (5–29%) | 1 ligoje |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Kartais (5–29%) | 1 ligoje |
| CHMP2Bcharged multivesicular body protein 2B | Kartais (5–29%) | 1 ligoje |
| CPLX1complexin 1 | Kartais (5–29%) | 1 ligoje |
| DAOD-amino acid oxidase | Kartais (5–29%) | 1 ligoje |
| DCTN1dynactin subunit 1 | Kartais (5–29%) | 1 ligoje |
| EHMT1euchromatic histone lysine methyltransferase 1 | Kartais (5–29%) | 1 ligoje |
| ERBB4erb-b2 receptor tyrosine kinase 4 | Kartais (5–29%) | 1 ligoje |
| FIG4FIG4 phosphoinositide 5-phosphatase | Kartais (5–29%) | 1 ligoje |
| FUSFUS RNA binding protein | Kartais (5–29%) | 1 ligoje |
| GJB1gap junction protein beta 1 | Kartais (5–29%) | 1 ligoje |
Rodyti dar 40 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| GLE1GLE1 RNA export mediator | Kartais (5–29%) | 1 ligoje |
| GLT8D1glycosyltransferase 8 domain containing 1 | Kartais (5–29%) | 1 ligoje |
| HNF1BHNF1 homeobox B | Kartais (5–29%) | 1 ligoje |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Kartais (5–29%) | 2 ligose |
| HNRNPA2B1heterogeneous nuclear ribonucleoprotein A2/B1 | Kartais (5–29%) | 1 ligoje |
| KMT2Clysine methyltransferase 2C | Kartais (5–29%) | 1 ligoje |
| LHX1LIM homeobox 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 |
| NOTCH3notch receptor 3 | Kartais (5–29%) | 1 ligoje |
| OPTNoptineurin | Kartais (5–29%) | 1 ligoje |
| PFN1profilin 1 | Kartais (5–29%) | 1 ligoje |
| PRPHperipherin | Kartais (5–29%) | 1 ligoje |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Kartais (5–29%) | 1 ligoje |
| PRRT2proline rich transmembrane protein 2 | Kartais (5–29%) | 1 ligoje |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Kartais (5–29%) | 1 ligoje |
| SCN8Asodium voltage-gated channel alpha subunit 8 | Kartais (5–29%) | 1 ligoje |
| SOD1superoxide dismutase 1 | Kartais (5–29%) | 1 ligoje |
| SQSTM1sequestosome 1 | Kartais (5–29%) | 2 ligose |
| TAF15TATA-box binding protein associated factor 15 | Kartais (5–29%) | 1 ligoje |
| TARDBPTAR DNA binding protein | Kartais (5–29%) | 1 ligoje |
| TBC1D24TBC1 domain family member 24 | Kartais (5–29%) | 1 ligoje |
| TBK1TANK binding kinase 1 | Kartais (5–29%) | 2 ligose |
| UBQLN2ubiquilin 2 | Kartais (5–29%) | 1 ligoje |
| UNC13Aunc-13 homolog A | Kartais (5–29%) | 1 ligoje |
| VAPBVAMP associated protein B and C | Kartais (5–29%) | 1 ligoje |
| VCPvalosin containing protein | Kartais (5–29%) | 2 ligose |
| IRAK1interleukin 1 receptor associated kinase 1 | Retai (1–4 %) | 1 ligoje |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Retai (1–4 %) | 1 ligoje |
| SPP1secreted phosphoprotein 1 | Retai (1–4 %) | 1 ligoje |
| STAT4signal transducer and activator of transcription 4 | Retai (1–4 %) | 1 ligoje |
| CNTNAP2contactin associated protein 2 | Neužfiksuota | 1 ligoje |
| FLCNfolliculin | Neužfiksuota | 1 ligoje |
| MAPTmicrotubule associated protein tau | Neužfiksuota | 2 ligose |
| MBD5methyl-CpG binding domain protein 5 | Neužfiksuota | 1 ligoje |
| RAI1retinoic acid induced 1 | Neužfiksuota | 1 ligoje |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Neužfiksuota | 1 ligoje |
| TM4SF20transmembrane 4 L six family member 20 | Neužfiksuota | 1 ligoje |
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.
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- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.17-8666dff2.
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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 480+ physician-ready reports.
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