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Merkmal
Abdominal bloating
Klinische Bezeichnung: Abdominal distention
Distention of the abdomen.
Zusammenfassung
- Auch genannt
- Abdominal swelling, Belly bloating, Bloating, Abdominal distension, Distended abdomen
- Körpersystem
- Abnormality of the digestive system
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Diese Seite als Daten
Hängen Sie .json an die Adresse der Seite an oder fordern Sie application/json an, um sie als JSON zu lesen.
library(jsonlite)
url <- "https://dantelabs.com/traits/abdominal-distention.json"
page <- fromJSON(url)
page$trait$nameAbdominal bloatingHP:0003270
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Lesen Sie die Gene aus, die mit Abdominal bloating zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
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Meinen Genome Test bestellen109 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.
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- Congenital Diarrhoeas & EnteropathiesReads 7 of these genesSLC9A3STX3EPCAMMYO5BSLC5A1SLC26A3About this report →
Show 105 more reports
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- Metachromatic LeukodystrophyReads 2 of these genesARSAPSAPAbout this report →
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 2 of these genesALKPHOX2BAbout this report →
- Congenital HypothyroidismReads 6 of these genesFOXE1NKX2-1NKX2-5PAX8SLC26A4TSHRAbout this report →
- Disorder of Copper MetabolismReads 2 of these genesATP7BATP7AAbout this report →
- Familial Hemiplegic MigraineReads 2 of these genesATP1A2CACNA1AAbout this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 2 of these genesPHOX2BRETAbout this report →
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- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
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- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
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- Curry-Jones Syndrome (Mosaic SMO Syndrome)Reads 1 of these genesSMOAbout this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- Glucose-Galactose MalabsorptionReads 1 of these genesSLC5A1About this report →
- Jeune Asphyxiating Thoracic Dystrophy (DYNC2H1)Reads 1 of these genesDYNC2H1About this report →
- Lysosomal Acid Lipase Deficiency (Wolman Disease and CESD)Reads 1 of these genesLIPAAbout this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- Pendred SyndromeReads 1 of these genesSLC26A4About this report →
- PLEC-Related Epidermolysis Bullosa and Muscular DystrophyReads 1 of these genesPLECAbout this report →
- Polycystic Ovary SyndromeReads 1 of these genesFSHRAbout this report →
- Short-Rib Thoracic Dysplasia 11 (DYNC2I2)Reads 1 of these genesDYNC2I2About this report →
- Short-Rib Thoracic Dysplasia 7 (WDR35)Reads 1 of these genesWDR35About this report →
- Short-Rib Thoracic Dysplasia 8 (DYNC2I1)Reads 1 of these genesDYNC2I1About this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Thyroid CancerReads 5 of these genesNKX2-5PAX8SLC26A4TSHRRETAbout this report →
- Waardenburg SyndromeReads 2 of these genesEDN3EDNRBAbout this report →
- Epilepsy (Full Panel)Reads 10 of these genesPIGAATP1A2ATP1A3CACNA1AHACE1RHOBTB2About this report →
- Hepatic Porphyria DisordersReads 2 of these genesALADHMBSAbout this report →
- Congenital Disaccharidase DeficienciesReads 1 of these genesSIAbout this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 1 of these genesBRCA1About this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesINSRAbout this report →
- TRIP11-Related Skeletal DysplasiaReads 1 of these genesTRIP11About this report →
- Epidermolysis BullosaReads 3 of these genesITGA6ITGB4PLECAbout this report →
- Primary Mitochondrial DiseaseReads 8 of these genesPOLG2LIG3POLGRRM2BTYMPC2orf69About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL2A1SLC26A2About this report →
- PorphyriaReads 2 of these genesALADHMBSAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 10 of these genesTRMULIG3POLGRRM2BTYMPATP7AAbout this report →
- Meckel SyndromeReads 2 of these genesTXNDC15TCTN2About this report →
- Fraser SyndromeReads 1 of these genesFREM2About this report →
- Hereditary Fructose Intolerance & Gluconeogenesis DefectsReads 1 of these genesALDOBAbout this report →
- HyperthyroidismReads 1 of these genesTSHRAbout this report →
- Immuno-Osseous DysplasiasReads 1 of these genesSMARCAL1About this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Aortic AneurysmReads 2 of these genesMYH11MYLKAbout this report →
- Inherited Congenital Heart DefectsReads 2 of these genesNKX2-5FLNAAbout this report →
- Lysosomal Storage DiseaseReads 4 of these genesLIPASMPD1ARSAPSAPAbout this report →
- Glycogen Storage DiseaseReads 2 of these genesSLC2A2PYGLAbout this report →
- Hereditary Vascular MalformationsReads 1 of these genesEPHB4About this report →
- Neonatal Diabetes MellitusReads 2 of these genesMNX1SLC2A2About this report →
- Lynch SyndromeReads 1 of these genesEPCAMAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesLRP5About this report →
- Syndromic CraniosynostosisReads 2 of these genesWDR35SMOAbout this report →
- Inherited Neurodegenerative DisordersReads 8 of these genesPOLGABCD1ATP1A3ATP7ACACNA1AHACE1About this report →
- Renal Tubular AcidosisReads 1 of these genesSLC4A1About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesNKX2-5About this report →
- Systemic Lupus ErythematosusReads 1 of these genesSAT1About this report →
- Congenital Disorders of GlycosylationReads 4 of these genesPIGAALG8DLL3MESP2About this report →
- VitreoretinopathyReads 2 of these genesCOL2A1LRP5About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesWDR35About this report →
- Hereditary HypolipoproteinemiasReads 1 of these genesSAR1BAbout this report →
- Diabetes MellitusReads 2 of these genesMNX1SLC2A2About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesRETAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesPLECTNPO3About this report →
- Other Inherited LeukodystrophiesReads 3 of these genesABCD1ARSAPSAPAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 2 of these genesATP1A3CACNA1AAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesATP1A3SLC2A1About this report →
- Autism Spectrum DisorderReads 1 of these genesCHD8About this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesCACNA1AAbout this report →
- Familial Intrahepatic CholestasisReads 1 of these genesMYO5BAbout this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesRETAbout this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 1 of these genesIL12RB1About this report →
- HyperinsulinismReads 1 of these genesINSRAbout this report →
- Polycystic Kidney DiseaseReads 1 of these genesALG8About this report →
- Urinary and Renal System TumourReads 1 of these genesRETAbout this report →
- Hereditary Optic NeuropathyReads 1 of these genesATP1A3About this report →
- OsteopetrosisReads 1 of these genesLRP5About this report →
- Cutis LaxaReads 1 of these genesATP7AAbout this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesEPHB4About this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesABCD1HACE1About this report →
- Fanconi AnemiaReads 1 of these genesBRCA1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesWT1About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesATP7AMPV17About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGAAbout this report →
- Autoimmune DiseaseReads 1 of these genesSAT1About this report →
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- Intellectual DisabilityReads 3 of these genesSCN2ACHD8ZEB2About this report →
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- Nephrotic SyndromeReads 1 of these genesNPHS1About this report →
- Inherited ThrombocytopeniasReads 1 of these genesFLI1About this report →
- Osteogenesis ImperfectaReads 1 of these genesLRP5About this report →
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Lesen Sie die Gene aus, die mit Abdominal bloating zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
Ab 449 $Kostenloser Versand · Ergebnisse in 6–8 Wochen
Meinen Genome Test bestellen135 Gene mit Abdominal bloating verknüpft
Veränderungen in diesen Genen verursachen seltene Erkrankungen, bei denen Abdominal bloating auftritt. Die meisten Menschen mit diesem Merkmal haben keine dieser Erkrankungen, und ein Gen auf dieser Liste sagt nichts über das eigene Genom einer Person aus.
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| ATP7BATPase copper transporting beta | Immer | In 1 Erkrankung |
| CLMPCXADR like cell adhesion molecule | Immer | In 1 Erkrankung |
| DHCR77-dehydrocholesterol reductase | Immer | In 1 Erkrankung |
| LIPAlipase A, lysosomal acid type | Immer | In 2 Erkrankungen |
| LMOD1leiomodin 1 | Immer | In 2 Erkrankungen |
| MYH11myosin heavy chain 11 | Immer | In 2 Erkrankungen |
| MYL9myosin light chain 9 | Immer | In 1 Erkrankung |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Immer | In 1 Erkrankung |
| PLD4phospholipase D family member 4 | Immer | In 1 Erkrankung |
| POLG2DNA polymerase gamma 2, accessory subunit | Immer | In 1 Erkrankung |
| SLC9A3solute carrier family 9 member A3 | Immer | In 1 Erkrankung |
| STX3syntaxin 3 | Immer | In 2 Erkrankungen |
| TRMUtRNA mitochondrial 2-thiouridylase | Immer | In 1 Erkrankung |
| TXNDC15thioredoxin domain containing 15 | Immer | In 1 Erkrankung |
| ACTG2actin gamma 2, smooth muscle | Sehr häufig (80–99 %) | In 3 Erkrankungen |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| BRCA1BRCA1 DNA repair associated | Sehr häufig (80–99 %) | In 1 Erkrankung |
| COL2A1collagen type II alpha 1 chain | Sehr häufig (80–99 %) | In 1 Erkrankung |
| DYNC2H1dynein cytoplasmic 2 heavy chain 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| DYNC2I1dynein 2 intermediate chain 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| DYNC2I2dynein 2 intermediate chain 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| EWSR1EWS RNA binding protein 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| FOXE1forkhead box E1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| FSHRfollicle stimulating hormone receptor | Sehr häufig (80–99 %) | In 1 Erkrankung |
| IFT80intraflagellar transport 80 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ITGA6integrin subunit alpha 6 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ITGB4integrin subunit beta 4 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| LIG3DNA ligase 3 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| LRP5LDL receptor related protein 5 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| MYLKmyosin light chain kinase | Sehr häufig (80–99 %) | In 1 Erkrankung |
| NKX2-1NK2 homeobox 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| NKX2-5NK2 homeobox 5 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| PAX8paired box 8 | Sehr häufig (80–99 %) | In 4 Erkrankungen |
| POLGDNA polymerase gamma, catalytic subunit | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| PRKCSHPRKCSH beta subunit of glucosidase II | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SEC63SEC63 protein translocation regulator | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SLC26A4solute carrier family 26 member 4 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| TRIP11thyroid hormone receptor interactor 11 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| TSHRthyroid stimulating hormone receptor | Sehr häufig (80–99 %) | In 2 Erkrankungen |
95 weitere Gene anzeigen
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| TYMPthymidine phosphorylase | Sehr häufig (80–99 %) | In 1 Erkrankung |
| WDR35WD repeat domain 35 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| WT1WT1 transcription factor | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ABCD1ATP binding cassette subfamily D member 1 | Häufig (30–79 %) | In 1 Erkrankung |
| ALKALK receptor tyrosine kinase | Häufig (30–79 %) | In 1 Erkrankung |
| ANO1anoctamin 1 | Häufig (30–79 %) | In 1 Erkrankung |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Häufig (30–79 %) | In 1 Erkrankung |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Häufig (30–79 %) | In 1 Erkrankung |
| ATP7AATPase copper transporting alpha | Häufig (30–79 %) | In 1 Erkrankung |
| C2orf69chromosome 2 open reading frame 69 | Häufig (30–79 %) | In 1 Erkrankung |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Häufig (30–79 %) | In 1 Erkrankung |
| COX11cytochrome c oxidase copper chaperone COX11 | Häufig (30–79 %) | In 1 Erkrankung |
| DYMdymeclin | Häufig (30–79 %) | In 1 Erkrankung |
| ECE1endothelin converting enzyme 1 | Häufig (30–79 %) | In 1 Erkrankung |
| EDN3endothelin 3 | Häufig (30–79 %) | In 1 Erkrankung |
| EDNRBendothelin receptor type B | Häufig (30–79 %) | In 1 Erkrankung |
| EPCAMepithelial cell adhesion molecule | Häufig (30–79 %) | In 1 Erkrankung |
| ERBB2erb-b2 receptor tyrosine kinase 2 | Häufig (30–79 %) | In 1 Erkrankung |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Häufig (30–79 %) | In 1 Erkrankung |
| FOCADfocadhesin | Häufig (30–79 %) | In 1 Erkrankung |
| GDNFglial cell derived neurotrophic factor | Häufig (30–79 %) | In 1 Erkrankung |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Häufig (30–79 %) | In 1 Erkrankung |
| INSRinsulin receptor | Häufig (30–79 %) | In 2 Erkrankungen |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | Häufig (30–79 %) | In 1 Erkrankung |
| LMO1LIM domain only 1 | Häufig (30–79 %) | In 1 Erkrankung |
| MNX1motor neuron and pancreas homeobox 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Häufig (30–79 %) | In 1 Erkrankung |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Häufig (30–79 %) | In 1 Erkrankung |
| MYO5Bmyosin VB | Häufig (30–79 %) | In 1 Erkrankung |
| NRTNneurturin | Häufig (30–79 %) | In 1 Erkrankung |
| PHOX2Bpaired like homeobox 2B | Häufig (30–79 %) | In 1 Erkrankung |
| PI4KAphosphatidylinositol 4-kinase alpha | Häufig (30–79 %) | In 1 Erkrankung |
| PLECplectin | Häufig (30–79 %) | In 1 Erkrankung |
| RETret proto-oncogene | Häufig (30–79 %) | In 2 Erkrankungen |
| RHOBTB2Rho related BTB domain containing 2 | Häufig (30–79 %) | In 1 Erkrankung |
| SAR1Bsecretion associated Ras related GTPase 1B | Häufig (30–79 %) | In 1 Erkrankung |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Häufig (30–79 %) | In 1 Erkrankung |
| SEMA3Csemaphorin 3C | Häufig (30–79 %) | In 1 Erkrankung |
| SEMA3Dsemaphorin 3D | Häufig (30–79 %) | In 1 Erkrankung |
| SLC1A3solute carrier family 1 member 3 | Häufig (30–79 %) | In 1 Erkrankung |
| SLC2A1solute carrier family 2 member 1 | Häufig (30–79 %) | In 1 Erkrankung |
| SLC2A2solute carrier family 2 member 2 | Häufig (30–79 %) | In 2 Erkrankungen |
| SLC5A1solute carrier family 5 member 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Häufig (30–79 %) | In 1 Erkrankung |
| SMOsmoothened, frizzled class receptor | Häufig (30–79 %) | In 1 Erkrankung |
| SMPD1sphingomyelin phosphodiesterase 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| SREBF1sterol regulatory element binding transcription factor 1 | Häufig (30–79 %) | In 1 Erkrankung |
| TCTN2tectonic family member 2 | Häufig (30–79 %) | In 1 Erkrankung |
| TFAMtranscription factor A, mitochondrial | Häufig (30–79 %) | In 1 Erkrankung |
| TTC7Atetratricopeptide repeat domain 7A | Häufig (30–79 %) | In 1 Erkrankung |
| AGR2anterior gradient 2, protein disulphide isomerase family member | Manchmal (5–29 %) | In 1 Erkrankung |
| ALADaminolevulinate dehydratase | Manchmal (5–29 %) | In 1 Erkrankung |
| ALDOBaldolase, fructose-bisphosphate B | Manchmal (5–29 %) | In 1 Erkrankung |
| ARSAarylsulfatase A | Manchmal (5–29 %) | In 3 Erkrankungen |
| CHD8chromodomain helicase DNA binding protein 8 | Manchmal (5–29 %) | In 1 Erkrankung |
| DDRGK1DDRGK domain containing 1 | Manchmal (5–29 %) | In 2 Erkrankungen |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Manchmal (5–29 %) | In 1 Erkrankung |
| HMBShydroxymethylbilane synthase | Manchmal (5–29 %) | In 1 Erkrankung |
| IFT56intraflagellar transport 56 | Manchmal (5–29 %) | In 1 Erkrankung |
| IL12Ainterleukin 12A | Manchmal (5–29 %) | In 1 Erkrankung |
| IL12RB1interleukin 12 receptor subunit beta 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| IPO8importin 8 | Manchmal (5–29 %) | In 1 Erkrankung |
| IRAK1interleukin 1 receptor associated kinase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| IRF5interferon regulatory factor 5 | Manchmal (5–29 %) | In 1 Erkrankung |
| MMEL1membrane metalloendopeptidase like 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| MPV17mitochondrial inner membrane protein MPV17 | Manchmal (5–29 %) | In 1 Erkrankung |
| POU2AF1POU class 2 homeobox associating factor 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| PSAPprosaposin | Manchmal (5–29 %) | In 3 Erkrankungen |
| PYGLglycogen phosphorylase L | Manchmal (5–29 %) | In 1 Erkrankung |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SIsucrase-isomaltase | Manchmal (5–29 %) | In 1 Erkrankung |
| SPIBSpi-B transcription factor | Manchmal (5–29 %) | In 1 Erkrankung |
| SPP1secreted phosphoprotein 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| STAT4signal transducer and activator of transcription 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| TNFSF15TNF superfamily member 15 | Manchmal (5–29 %) | In 1 Erkrankung |
| TNPO3transportin 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| TREHtrehalase | Manchmal (5–29 %) | In 1 Erkrankung |
| ANK1ankyrin 1 | Selten (1–4 %) | In 1 Erkrankung |
| EPB42erythrocyte membrane protein band 4.2 | Selten (1–4 %) | In 1 Erkrankung |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Selten (1–4 %) | In 1 Erkrankung |
| SPTA1spectrin alpha, erythrocytic 1 | Selten (1–4 %) | In 1 Erkrankung |
| SPTBspectrin beta, erythrocytic | Selten (1–4 %) | In 1 Erkrankung |
| DLL3delta like canonical Notch ligand 3 | Nicht erfasst | In 1 Erkrankung |
| EPHB4EPH receptor B4 | Nicht erfasst | In 1 Erkrankung |
| FLNAfilamin A | Nicht erfasst | In 1 Erkrankung |
| FREM2FRAS1 related extracellular matrix 2 | Nicht erfasst | In 1 Erkrankung |
| HLA-DQA1major histocompatibility complex, class II, DQ alpha 1 | Nicht erfasst | In 1 Erkrankung |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Nicht erfasst | In 1 Erkrankung |
| KRT18keratin 18 | Nicht erfasst | In 1 Erkrankung |
| MESP2mesoderm posterior bHLH transcription factor 2 | Nicht erfasst | In 1 Erkrankung |
| NPHS1NPHS1 adhesion molecule, nephrin | Nicht erfasst | In 1 Erkrankung |
| SLC26A2solute carrier family 26 member 2 | Nicht erfasst | In 1 Erkrankung |
| SLC26A3solute carrier family 26 member 3 | Nicht erfasst | In 1 Erkrankung |
| SPINT2serine peptidase inhibitor, Kunitz type 2 | Nicht erfasst | In 1 Erkrankung |
| ZEB2zinc finger E-box binding homeobox 2 | Nicht erfasst | In 1 Erkrankung |
Wie häufig dieses Merkmal bei Menschen mit einer der Erkrankungen auftritt, die mit dem Gen in Verbindung stehen, und zwar der höchste Wert unter ihnen, so wie ihn die Human Phenotype Ontology erfasst. Diese Seiten beschreiben Merkmale und die dazugehörige Forschung; sie stellen keine Diagnose dar. Fragen zu Symptomen richten Sie bitte an Ihre Ärztin, Ihren Arzt oder eine genetische Beratung.
Untergeordnete Merkmale
Übergeordnete Merkmale
Woher diese Angaben stammen
- Die Human Phenotype Ontology, Version 2026-09-01: das Merkmal, seine Bezeichnungen, seine Definition und die damit verknüpften Gene. Weitere Informationen finden Sie unter hpo.jax.org.
- Datenstand 2026.10.19-9814e911.
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