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Piirre
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.
Yhteenveto
- Tunnetaan myös nimellä
- Language disorder
- Elimistön järjestelmä
- Abnormality of the nervous system
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Tämä sivu datana
Lisää sivun osoitteen perään .json tai pyydä application/json-muotoa, niin saat sivun JSON-muodossa.
library(jsonlite)
url <- "https://dantelabs.com/traits/language-impairment.json"
page <- fromJSON(url)
page$trait$nameLanguage impairmentHP:0002463
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
Lue Language impairment-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
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Tilaa Genome Test49 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 45 more reports
- Inherited Neurodegenerative DisordersReads 29 of these genesABCB7APPPSEN1PSEN2TREM2ANGAbout this report →
- Distal MyopathiesReads 5 of these genesHNRNPA1HNRNPA2B1LRP12MATR3VCPAbout this report →
- Amyotrophic Lateral Sclerosis Susceptibility 24 (NEK1)Reads 1 of these genesNEK1About this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
- BCKDK DeficiencyReads 1 of these genesBCKDKAbout this report →
- Birt-Hogg-Dubé SyndromeReads 1 of these genesFLCNAbout this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- OPTN-Related Normal-Tension GlaucomaReads 1 of these genesOPTNAbout this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- DOORS SyndromeReads 1 of these genesTBC1D24About 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 →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesGRHL3About 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 →
- Rare Hereditary Peripheral NeuropathiesReads 7 of these genesCHCHD10DCTN1FIG4GJB1NEFHPRPS1About this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 1 of these genesHNF1BAbout this report →
- Lissencephaly Spectrum DisordersReads 2 of these genesDCXPAFAH1B1About 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 →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesCACNA1AAbout 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 →
Lue Language impairment-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
Alkaen 449 $Ilmainen toimitus · Tulokset 6–8 viikossa
Tilaa Genome Test80 geeniä, jotka liittyvät piirteeseen Language impairment
Näiden geenien muutokset aiheuttavat harvinaisia sairauksia, joissa Language impairment esiintyy. Useimmilla, joilla on tämä piirre, ei ole mitään näistä sairauksista, eikä tämän listan geeni kerro mitään kenenkään omasta genomista.
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| ABCB7ATP binding cassette subfamily B member 7 | Aina | 1 sairaudessa |
| ADGRG1adhesion G protein-coupled receptor G1 | Aina | 3 sairaudessa |
| BCKDKbranched chain keto acid dehydrogenase kinase | Aina | 1 sairaudessa |
| FOXP1forkhead box P1 | Aina | 1 sairaudessa |
| GATAD2BGATA zinc finger domain containing 2B | Aina | 1 sairaudessa |
| APPamyloid beta precursor protein | Hyvin usein (80–99%) | 1 sairaudessa |
| BCRBCR activator of RhoGEF and GTPase | Hyvin usein (80–99%) | 1 sairaudessa |
| CRKLCRK like proto-oncogene, adaptor protein | Hyvin usein (80–99%) | 1 sairaudessa |
| DCXdoublecortin | Hyvin usein (80–99%) | 1 sairaudessa |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Hyvin usein (80–99%) | 1 sairaudessa |
| MAPK1mitogen-activated protein kinase 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| PSEN1presenilin 1 | Hyvin usein (80–99%) | 3 sairaudessa |
| PSEN2presenilin 2 | Hyvin usein (80–99%) | 1 sairaudessa |
| SORL1sortilin related receptor 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| TOMM40translocase of outer mitochondrial membrane 40 | Hyvin usein (80–99%) | 1 sairaudessa |
| TREM2triggering receptor expressed on myeloid cells 2 | Hyvin usein (80–99%) | 2 sairaudessa |
| GRHL3grainyhead like transcription factor 3 | Usein (30–79%) | 1 sairaudessa |
| NF1neurofibromin 1 | Usein (30–79%) | 1 sairaudessa |
| PAFAH1B1platelet activating factor acetylhydrolase 1b regulatory subunit 1 | Usein (30–79%) | 1 sairaudessa |
| PI4KAphosphatidylinositol 4-kinase alpha | Usein (30–79%) | 1 sairaudessa |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | Usein (30–79%) | 1 sairaudessa |
| SRPX2sushi repeat containing protein X-linked 2 | Usein (30–79%) | 1 sairaudessa |
| UBBubiquitin B | Usein (30–79%) | 1 sairaudessa |
| ANGangiogenin | Joskus (5–29%) | 1 sairaudessa |
| ANXA11annexin A11 | Joskus (5–29%) | 1 sairaudessa |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Joskus (5–29%) | 1 sairaudessa |
| ATXN2ataxin 2 | Joskus (5–29%) | 1 sairaudessa |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Joskus (5–29%) | 1 sairaudessa |
| CCNFcyclin F | Joskus (5–29%) | 1 sairaudessa |
| CFAP410cilia and flagella associated protein 410 | Joskus (5–29%) | 1 sairaudessa |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Joskus (5–29%) | 1 sairaudessa |
| CHMP2Bcharged multivesicular body protein 2B | Joskus (5–29%) | 1 sairaudessa |
| CPLX1complexin 1 | Joskus (5–29%) | 1 sairaudessa |
| DAOD-amino acid oxidase | Joskus (5–29%) | 1 sairaudessa |
| DCTN1dynactin subunit 1 | Joskus (5–29%) | 1 sairaudessa |
| EHMT1euchromatic histone lysine methyltransferase 1 | Joskus (5–29%) | 1 sairaudessa |
| ERBB4erb-b2 receptor tyrosine kinase 4 | Joskus (5–29%) | 1 sairaudessa |
| FIG4FIG4 phosphoinositide 5-phosphatase | Joskus (5–29%) | 1 sairaudessa |
| FUSFUS RNA binding protein | Joskus (5–29%) | 1 sairaudessa |
| GJB1gap junction protein beta 1 | Joskus (5–29%) | 1 sairaudessa |
Näytä 40 geeniä lisää
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| GLE1GLE1 RNA export mediator | Joskus (5–29%) | 1 sairaudessa |
| GLT8D1glycosyltransferase 8 domain containing 1 | Joskus (5–29%) | 1 sairaudessa |
| HNF1BHNF1 homeobox B | Joskus (5–29%) | 1 sairaudessa |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Joskus (5–29%) | 2 sairaudessa |
| HNRNPA2B1heterogeneous nuclear ribonucleoprotein A2/B1 | Joskus (5–29%) | 1 sairaudessa |
| KMT2Clysine methyltransferase 2C | Joskus (5–29%) | 1 sairaudessa |
| LHX1LIM homeobox 1 | Joskus (5–29%) | 1 sairaudessa |
| LRP12LDL receptor related protein 12 | Joskus (5–29%) | 1 sairaudessa |
| MATR3matrin 3 | Joskus (5–29%) | 1 sairaudessa |
| NEFHneurofilament heavy chain | Joskus (5–29%) | 1 sairaudessa |
| NEK1NIMA related kinase 1 | Joskus (5–29%) | 1 sairaudessa |
| NOTCH3notch receptor 3 | Joskus (5–29%) | 1 sairaudessa |
| OPTNoptineurin | Joskus (5–29%) | 1 sairaudessa |
| PFN1profilin 1 | Joskus (5–29%) | 1 sairaudessa |
| PRPHperipherin | Joskus (5–29%) | 1 sairaudessa |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Joskus (5–29%) | 1 sairaudessa |
| PRRT2proline rich transmembrane protein 2 | Joskus (5–29%) | 1 sairaudessa |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Joskus (5–29%) | 1 sairaudessa |
| SCN8Asodium voltage-gated channel alpha subunit 8 | Joskus (5–29%) | 1 sairaudessa |
| SOD1superoxide dismutase 1 | Joskus (5–29%) | 1 sairaudessa |
| SQSTM1sequestosome 1 | Joskus (5–29%) | 2 sairaudessa |
| TAF15TATA-box binding protein associated factor 15 | Joskus (5–29%) | 1 sairaudessa |
| TARDBPTAR DNA binding protein | Joskus (5–29%) | 1 sairaudessa |
| TBC1D24TBC1 domain family member 24 | Joskus (5–29%) | 1 sairaudessa |
| TBK1TANK binding kinase 1 | Joskus (5–29%) | 2 sairaudessa |
| UBQLN2ubiquilin 2 | Joskus (5–29%) | 1 sairaudessa |
| UNC13Aunc-13 homolog A | Joskus (5–29%) | 1 sairaudessa |
| VAPBVAMP associated protein B and C | Joskus (5–29%) | 1 sairaudessa |
| VCPvalosin containing protein | Joskus (5–29%) | 2 sairaudessa |
| IRAK1interleukin 1 receptor associated kinase 1 | Harvinainen (1–4 %) | 1 sairaudessa |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Harvinainen (1–4 %) | 1 sairaudessa |
| SPP1secreted phosphoprotein 1 | Harvinainen (1–4 %) | 1 sairaudessa |
| STAT4signal transducer and activator of transcription 4 | Harvinainen (1–4 %) | 1 sairaudessa |
| CNTNAP2contactin associated protein 2 | Ei kirjattu | 1 sairaudessa |
| FLCNfolliculin | Ei kirjattu | 1 sairaudessa |
| MAPTmicrotubule associated protein tau | Ei kirjattu | 2 sairaudessa |
| MBD5methyl-CpG binding domain protein 5 | Ei kirjattu | 1 sairaudessa |
| RAI1retinoic acid induced 1 | Ei kirjattu | 1 sairaudessa |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Ei kirjattu | 1 sairaudessa |
| TM4SF20transmembrane 4 L six family member 20 | Ei kirjattu | 1 sairaudessa |
Kuinka usein ilmiö esiintyy ihmisillä, joilla on jokin geenin sairauksista, niin kuin Human Phenotype Ontology sen kirjaa. Nämä sivut kuvaavat piirteitä ja niiden taustalla olevaa tutkimusta, eivätkä ne ole diagnoosi. Oireista kannattaa kysyä lääkäriltä tai geneettiseltä neuvojalta.
Tarkemmat piirteet
Laajemmat piirteet
Mistä tämä tieto tulee
- Human Phenotype Ontology, julkaisu 2026-09-01: piirre, sen nimet, määritelmä ja siihen liitetyt geenit. Lue lisää osoitteesta hpo.jax.org.
- Tietojulkaisu 2026.10.18-8b139e39.
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
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.
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