AtlasTræk
Intellectual disability, borderline
Klinisk navn: Borderline intellectual disability
Borderline intellectual disability is defined as an intelligence quotient (IQ) in the range of 70-85.
Resumé
- Kropssystem
- Abnormality of the nervous system
AtlasDenne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/borderline-intellectual-disability.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Intellectual disability, borderline, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test24 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.
- HyperlysinaemiaReads 1 of these genesAASSAbout this report →
- MDPL SyndromeReads 1 of these genesPOLD1About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 2 of these genesMAGEL2SNRPNAbout this report →
- Inherited IchthyosesReads 2 of these genesALOX12BALOXE3About this report →
Show 20 more reports
- Colorectal Cancer & PolyposisReads 1 of these genesPOLD1About this report →
- Epilepsy (Full Panel)Reads 5 of these genesSCN8AGABRG2GRIN2AKCNMA1SCN3AAbout this report →
- Oculocutaneous AlbinismReads 1 of these genesOCA2About this report →
- Autism Spectrum DisorderReads 1 of these genesCHD8About this report →
- Hypogonadotropic HypogonadismReads 2 of these genesMAGEL2SNRPNAbout this report →
- Intellectual DisabilityReads 4 of these genesCHD8DHX9SRPK3TRIOAbout this report →
- Noonan SyndromeReads 1 of these genesNRASAbout this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesIFT172About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesPAN2About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesCLDN11About this report →
- Congenital Muscular DystrophiesReads 1 of these genesPOMKAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesTRAPPC11About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesNRASAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesENTPD1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesDHX9About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesCLDN11About this report →
- Retinitis PigmentosaReads 1 of these genesIFT172About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesCLDN11ENTPD1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesPOLD1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesDHX9About this report →
Læs de gener, der er knyttet til Intellectual disability, borderline, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test31 gener knyttet til Intellectual disability, borderline
Ændringer i disse gener forårsager sjældne tilstande, hvor Intellectual disability, borderline ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| CACHD1cache domain containing 1 | Altid | I 1 tilstand |
| CLDN11claudin 11 | Altid | I 1 tilstand |
| IFT172intraflagellar transport 172 | Altid | I 1 tilstand |
| NUDT2nudix hydrolase 2 | Altid | I 1 tilstand |
| POMKprotein O-mannose kinase | Altid | I 1 tilstand |
| RAB3ARAB3A, member RAS oncogene family | Altid | I 1 tilstand |
| YY1AP1YY1 associated protein 1 | Meget ofte (80–99 %) | I 1 tilstand |
| ENTPD1ectonucleoside triphosphate diphosphohydrolase 1 | Ofte (30–79 %) | I 1 tilstand |
| MAGEL2MAGE family member L2 | Ofte (30–79 %) | I 4 tilstande |
| NDNnecdin, MAGE family member | Ofte (30–79 %) | I 3 tilstande |
| NRASNRAS proto-oncogene, GTPase | Ofte (30–79 %) | I 1 tilstand |
| OCA2OCA2 melanosomal transmembrane protein | Ofte (30–79 %) | I 3 tilstande |
| POLD1DNA polymerase delta 1, catalytic subunit | Ofte (30–79 %) | I 1 tilstand |
| SCN8Asodium voltage-gated channel alpha subunit 8 | Ofte (30–79 %) | I 1 tilstand |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Ofte (30–79 %) | I 3 tilstande |
| TRAPPC11trafficking protein particle complex subunit 11 | Ofte (30–79 %) | I 1 tilstand |
| AASSaminoadipate-semialdehyde synthase | Nogle gange (5–29 %) | I 1 tilstand |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Nogle gange (5–29 %) | I 1 tilstand |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Nogle gange (5–29 %) | I 1 tilstand |
| CHD8chromodomain helicase DNA binding protein 8 | Nogle gange (5–29 %) | I 1 tilstand |
| DHX9DExH-box helicase 9 | Nogle gange (5–29 %) | I 1 tilstand |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Nogle gange (5–29 %) | I 1 tilstand |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Nogle gange (5–29 %) | I 1 tilstand |
| KCNMA1potassium calcium-activated channel subfamily M alpha 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MAU2MAU2 sister chromatid cohesion factor | Nogle gange (5–29 %) | I 1 tilstand |
| PAN2poly(A) specific ribonuclease subunit PAN2 | Nogle gange (5–29 %) | I 1 tilstand |
| SCN3Asodium voltage-gated channel alpha subunit 3 | Nogle gange (5–29 %) | I 1 tilstand |
| SRPK3SRSF protein kinase 3 | Nogle gange (5–29 %) | I 1 tilstand |
| SRPX2sushi repeat containing protein X-linked 2 | Nogle gange (5–29 %) | I 1 tilstand |
| TONSLtonsoku like, DNA repair protein | Nogle gange (5–29 %) | I 1 tilstand |
| TRIOtrio Rho guanine nucleotide exchange factor | Nogle gange (5–29 %) | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
AtlasFrom traits to your genome
Read the genes behind these traits in your own DNA.
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