AtlasKenmerk
Laryngospasm
A spasm (involuntary contraction) of the vocal cords that can make it difficult to speak or breathe.
Samenvatting
- Lichaamssysteem
- Abnormality of the respiratory system
AtlasDeze pagina als gegevens
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library(jsonlite)
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page$trait$nameLees de genen die aan Laryngospasm gekoppeld zijn, en de rest van uw genoom, met één test.
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Mijn Genome Test bestellen30 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 7 of these genesCCNFCHCHD10CHMP2BHNRNPA1SQSTM1TBK1About this report →
- Inherited Neurodegenerative DisordersReads 22 of these genesANGANXA11ATXN2CCNFCHCHD10CHMP2BAbout this report →
- Amyotrophic Lateral Sclerosis Susceptibility 24 (NEK1)Reads 1 of these genesNEK1About this report →
Show 26 more reports
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- OPTN-Related Normal-Tension GlaucomaReads 1 of these genesOPTNAbout this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- Distal MyopathiesReads 4 of these genesHNRNPA1LRP12MATR3VCPAbout this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout 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 →
- Charcot-Marie-Tooth DiseaseReads 4 of these genesDCTN1FIG4NEFHVCPAbout this report →
- Alzheimer diseaseReads 1 of these genesTREM2About this report →
- Spinal Muscular AtrophyReads 2 of these genesCHCHD10DCTN1About this report →
- Hyper-IgE SyndromeReads 1 of these genesSPINK5About this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 1 of these genesCASRAbout this report →
- GlaucomaReads 1 of these genesOPTNAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 5 of these genesCHCHD10DCTN1FIG4NEFHVCPAbout this report →
- Parkinson DiseaseReads 1 of these genesGBA1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesTSPYL1About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesSCN4AAbout this report →
- Thyroid CancerReads 1 of these genesCASRAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesATXN2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesSCN4AAbout this report →
- Epilepsy (Full Panel)Reads 2 of these genesGABRG2GRIN2AAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesGBA1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesTREM2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesSPINK5About this report →
- Intellectual DisabilityReads 1 of these genesERBB4About this report →
Lees de genen die aan Laryngospasm gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen40 genen gekoppeld aan Laryngospasm
Veranderingen in deze genen veroorzaken zeldzame aandoeningen waarbij Laryngospasm 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 |
|---|---|---|
| SPINK5serine peptidase inhibitor Kazal type 5 | Altijd | In 1 aandoening |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Vaak (30–79%) | In 1 aandoening |
| GBA1glucosylceramidase beta 1 | Vaak (30–79%) | In 1 aandoening |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Vaak (30–79%) | In 1 aandoening |
| SRPX2sushi repeat containing protein X-linked 2 | Vaak (30–79%) | In 1 aandoening |
| CASRcalcium sensing receptor | Soms (5–29%) | In 1 aandoening |
| ANGangiogenin | Zelden (1–4%) | In 1 aandoening |
| ANXA11annexin A11 | Zelden (1–4%) | In 1 aandoening |
| ATXN2ataxin 2 | Zelden (1–4%) | In 1 aandoening |
| CCNFcyclin F | Zelden (1–4%) | In 1 aandoening |
| CFAP410cilia and flagella associated protein 410 | Zelden (1–4%) | In 1 aandoening |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Zelden (1–4%) | In 1 aandoening |
| CHMP2Bcharged multivesicular body protein 2B | Zelden (1–4%) | In 1 aandoening |
| DAOD-amino acid oxidase | Zelden (1–4%) | In 1 aandoening |
| DCTN1dynactin subunit 1 | Zelden (1–4%) | In 1 aandoening |
| ERBB4erb-b2 receptor tyrosine kinase 4 | Zelden (1–4%) | In 1 aandoening |
| FIG4FIG4 phosphoinositide 5-phosphatase | Zelden (1–4%) | In 1 aandoening |
| FUSFUS RNA binding protein | Zelden (1–4%) | In 1 aandoening |
| GLE1GLE1 RNA export mediator | Zelden (1–4%) | In 1 aandoening |
| GLT8D1glycosyltransferase 8 domain containing 1 | Zelden (1–4%) | In 1 aandoening |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Zelden (1–4%) | In 1 aandoening |
| LRP12LDL receptor related protein 12 | Zelden (1–4%) | In 1 aandoening |
| MATR3matrin 3 | Zelden (1–4%) | In 1 aandoening |
| NEFHneurofilament heavy chain | Zelden (1–4%) | In 1 aandoening |
| NEK1NIMA related kinase 1 | Zelden (1–4%) | In 1 aandoening |
| OPTNoptineurin | Zelden (1–4%) | In 1 aandoening |
| PFN1profilin 1 | Zelden (1–4%) | In 1 aandoening |
| PRPHperipherin | Zelden (1–4%) | In 1 aandoening |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Zelden (1–4%) | In 2 aandoeningen |
| SOD1superoxide dismutase 1 | Zelden (1–4%) | In 1 aandoening |
| SQSTM1sequestosome 1 | Zelden (1–4%) | In 1 aandoening |
| TAF15TATA-box binding protein associated factor 15 | Zelden (1–4%) | In 1 aandoening |
| TARDBPTAR DNA binding protein | Zelden (1–4%) | In 1 aandoening |
| TBK1TANK binding kinase 1 | Zelden (1–4%) | In 1 aandoening |
| TREM2triggering receptor expressed on myeloid cells 2 | Zelden (1–4%) | In 1 aandoening |
| UBQLN2ubiquilin 2 | Zelden (1–4%) | In 1 aandoening |
| UNC13Aunc-13 homolog A | Zelden (1–4%) | In 1 aandoening |
| VAPBVAMP associated protein B and C | Zelden (1–4%) | In 1 aandoening |
| VCPvalosin containing protein | Zelden (1–4%) | In 1 aandoening |
| TSPYL1TSPY like 1 | Niet vastgelegd | 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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