AtlasKenmerk
Intellectual disability, borderline
Klinische naam: Borderline intellectual disability
Borderline intellectual disability is defined as an intelligence quotient (IQ) in the range of 70-85.
Samenvatting
- Lichaamssysteem
- Abnormality of the nervous system
AtlasDeze pagina als gegevens
Voeg .json toe aan het adres van de pagina, of vraag application/json aan, om haar als JSON te lezen.
library(jsonlite)
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page <- fromJSON(url)
page$trait$nameLees de genen die aan Intellectual disability, borderline gekoppeld zijn, en de rest van uw genoom, met één test.
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Mijn Genome Test bestellen24 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 →
Lees de genen die aan Intellectual disability, borderline gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen31 genen gekoppeld aan Intellectual disability, borderline
Veranderingen in deze genen veroorzaken zeldzame aandoeningen waarbij Intellectual disability, borderline voorkomt. De meeste mensen met dit kenmerk hebben geen van die aandoeningen, en een gen op deze lijst zegt niets over het eigen genoom van iemand.
| Gen | Hoe vaak het voorkomt | Aandoeningen |
|---|---|---|
| CACHD1cache domain containing 1 | Altijd | In 1 aandoening |
| CLDN11claudin 11 | Altijd | In 1 aandoening |
| IFT172intraflagellar transport 172 | Altijd | In 1 aandoening |
| NUDT2nudix hydrolase 2 | Altijd | In 1 aandoening |
| POMKprotein O-mannose kinase | Altijd | In 1 aandoening |
| RAB3ARAB3A, member RAS oncogene family | Altijd | In 1 aandoening |
| YY1AP1YY1 associated protein 1 | Heel vaak (80–99%) | In 1 aandoening |
| ENTPD1ectonucleoside triphosphate diphosphohydrolase 1 | Vaak (30–79%) | In 1 aandoening |
| MAGEL2MAGE family member L2 | Vaak (30–79%) | In 4 aandoeningen |
| NDNnecdin, MAGE family member | Vaak (30–79%) | In 3 aandoeningen |
| NRASNRAS proto-oncogene, GTPase | Vaak (30–79%) | In 1 aandoening |
| OCA2OCA2 melanosomal transmembrane protein | Vaak (30–79%) | In 3 aandoeningen |
| POLD1DNA polymerase delta 1, catalytic subunit | Vaak (30–79%) | In 1 aandoening |
| SCN8Asodium voltage-gated channel alpha subunit 8 | Vaak (30–79%) | In 1 aandoening |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Vaak (30–79%) | In 3 aandoeningen |
| TRAPPC11trafficking protein particle complex subunit 11 | Vaak (30–79%) | In 1 aandoening |
| AASSaminoadipate-semialdehyde synthase | Soms (5–29%) | In 1 aandoening |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Soms (5–29%) | In 1 aandoening |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Soms (5–29%) | In 1 aandoening |
| CHD8chromodomain helicase DNA binding protein 8 | Soms (5–29%) | In 1 aandoening |
| DHX9DExH-box helicase 9 | Soms (5–29%) | In 1 aandoening |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Soms (5–29%) | In 1 aandoening |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Soms (5–29%) | In 1 aandoening |
| KCNMA1potassium calcium-activated channel subfamily M alpha 1 | Soms (5–29%) | In 1 aandoening |
| MAU2MAU2 sister chromatid cohesion factor | Soms (5–29%) | In 1 aandoening |
| PAN2poly(A) specific ribonuclease subunit PAN2 | Soms (5–29%) | In 1 aandoening |
| SCN3Asodium voltage-gated channel alpha subunit 3 | Soms (5–29%) | In 1 aandoening |
| SRPK3SRSF protein kinase 3 | Soms (5–29%) | In 1 aandoening |
| SRPX2sushi repeat containing protein X-linked 2 | Soms (5–29%) | In 1 aandoening |
| TONSLtonsoku like, DNA repair protein | Soms (5–29%) | In 1 aandoening |
| TRIOtrio Rho guanine nucleotide exchange factor | Soms (5–29%) | In 1 aandoening |
Hoe vaak dit voorkomt bij mensen met een van de aandoeningen van het gen, de hoogste frequentie binnen die aandoeningen, zoals de Human Phenotype Ontology dit vastlegt. Deze pagina's beschrijven kenmerken en het onderzoek erachter; het zijn geen diagnose, en over symptomen kunt u het best een arts of genetisch adviseur raadplegen.
Bredere kenmerken
Waar dit vandaan komt
- De Human Phenotype Ontology, release 2026-09-01: het kenmerk, de namen, de definitie en de genen die ermee verbonden zijn. Meer informatie vindt u op hpo.jax.org.
- Gegevensrelease 2026.10.19-9814e911.
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