AtlasTræk
Intestinal pseudo-obstruction
A functional rather than mechanical obstruction of the intestines, associated with manifestations that resemble those caused by an intestinal obstruction, including distension, abdominal pain, nausea, vomiting, constipation or diarrhea, in an individual in whom a mechanical blockage has been excluded.
Resumé
- Også kaldet
- Intestinal pseudoobstruction
- Kropssystem
- Abnormality of the digestive 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/intestinal-pseudo-obstruction.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Intestinal pseudo-obstruction, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min 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.
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 4 of these genesERBB3MYH11ACTG2FLNAAbout this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Hereditary Optic NeuropathyReads 4 of these genesMT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Au-Kline SyndromeReads 1 of these genesHNRNPKAbout this report →
Show 34 more reports
- Curry-Jones Syndrome (Mosaic SMO Syndrome)Reads 1 of these genesSMOAbout this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- Mucopolysaccharidosis Type II (Hunter Syndrome)Reads 1 of these genesIDSAbout this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- Fanconi AnemiaReads 3 of these genesBRCA1BRCA2PALB2About this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- MelanomaReads 1 of these genesCDKN2AAbout this report →
- Leigh SyndromeReads 4 of these genesMT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Rare Hereditary Peripheral NeuropathiesReads 7 of these genesLIG3POLGTYMPMT-ND1MT-ND4MT-ND5About this report →
- DNA Repair DiseaseReads 3 of these genesBRCA1BRCA2PALB2About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Cornelia de Lange SyndromeReads 1 of these genesRAD21About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Malignant Endocrine NeoplasmReads 1 of these genesTP53About this report →
- Primary Mitochondrial DiseaseReads 4 of these genesLIG3POLGTYMPTWNKAbout this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 1 of these genesPALB2About this report →
- Kidney CancerReads 1 of these genesTP53About this report →
- Inherited Neurodegenerative DisordersReads 6 of these genesPOLGMT-ND1MT-ND4MT-ND5MT-ND6TWNKAbout this report →
- Urinary and Renal System TumourReads 1 of these genesTP53About this report →
- Aortic AneurysmReads 1 of these genesMYH11About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Noonan SyndromeReads 1 of these genesKRASAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesSMOAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesSMOAbout this report →
- Diabetes MellitusReads 1 of these genesMT-TL1About this report →
- Female InfertilityReads 1 of these genesTWNKAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesTWNKAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesIDSAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesKRASAbout this report →
- Epilepsy (Full Panel)Reads 1 of these genesFLNAAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesKRASAbout this report →
- Intellectual DisabilityReads 1 of these genesSMAD4About this report →
Læs de gener, der er knyttet til Intestinal pseudo-obstruction, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test36 gener knyttet til Intestinal pseudo-obstruction
Ændringer i disse gener forårsager sjældne tilstande, hvor Intestinal pseudo-obstruction 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 |
|---|---|---|
| LIG3DNA ligase 3 | Altid | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Altid | I 4 tilstande |
| RAD21RAD21 cohesin complex component | Altid | I 1 tilstand |
| SGO1shugoshin 1 | Altid | I 1 tilstand |
| BRCA1BRCA1 DNA repair associated | Ofte (30–79 %) | I 1 tilstand |
| BRCA2BRCA2 DNA repair associated | Ofte (30–79 %) | I 1 tilstand |
| CDKN2Acyclin dependent kinase inhibitor 2A | Ofte (30–79 %) | I 1 tilstand |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Ofte (30–79 %) | I 1 tilstand |
| KRASKRas proto-oncogene, GTPase | Ofte (30–79 %) | I 1 tilstand |
| PALB2partner and localizer of BRCA2 | Ofte (30–79 %) | I 1 tilstand |
| PALLDpalladin, cytoskeletal associated protein | Ofte (30–79 %) | I 1 tilstand |
| RABL3RAB, member of RAS oncogene family like 3 | Ofte (30–79 %) | I 1 tilstand |
| SMAD4SMAD family member 4 | Ofte (30–79 %) | I 1 tilstand |
| TP53tumor protein p53 | Ofte (30–79 %) | I 1 tilstand |
| TYMPthymidine phosphorylase | Ofte (30–79 %) | I 1 tilstand |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Nogle gange (5–29 %) | I 2 tilstande |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Nogle gange (5–29 %) | I 1 tilstand |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Nogle gange (5–29 %) | I 1 tilstand |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Nogle gange (5–29 %) | I 1 tilstand |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Nogle gange (5–29 %) | I 1 tilstand |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Nogle gange (5–29 %) | I 1 tilstand |
| MYH11myosin heavy chain 11 | Nogle gange (5–29 %) | I 1 tilstand |
| SMOsmoothened, frizzled class receptor | Nogle gange (5–29 %) | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Nogle gange (5–29 %) | I 2 tilstande |
| ACTG2actin gamma 2, smooth muscle | Ikke registreret | I 1 tilstand |
| FLNAfilamin A | Ikke registreret | I 1 tilstand |
| IDSiduronate 2-sulfatase | Ikke registreret | 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.
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Gratis forsendelse · Resultater på 6–8 uger
