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Merkmal
Mitral valve prolapse
One or both of the leaflets (cusps) of the mitral valve bulges back into the left atrium upon contraction of the left ventricle.
Zusammenfassung
- Körpersystem
- Abnormality of the cardiovascular system
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Hängen Sie .json an die Adresse der Seite an oder fordern Sie application/json an, um sie als JSON zu lesen.
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page$trait$nameMitral valve prolapseHP:0001634
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Meinen Genome Test bestellen70 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.
- Ehlers-Danlos SyndromeReads 13 of these genesAEBP1COL3A1B3GALT6CHST14COL1A2PLOD1About this report →
- Marfan Like SyndromesReads 8 of these genesFBN1FBN2SKIBGNSMAD3TGFB2About this report →
- Polycystic Kidney DiseaseReads 8 of these genesALG5ALG9DNAJB11GANABIFT140NEK8About this report →
- Noonan SyndromeReads 9 of these genesLZTR1BRAFHRASKRASPTPN11RAF1About this report →
Show 66 more reports
- Loeys-Dietz SyndromeReads 4 of these genesSMAD3TGFB2TGFBR1TGFBR2About this report →
- Congenital MyopathiesReads 7 of these genesRYR1MYH7MYPNSELENONTPM2TPM3About this report →
- Hypertrophic CardiomyopathyReads 11 of these genesLZTR1BRAFHRASKRASPTPN11RAF1About this report →
- Aortic AneurysmReads 5 of these genesFBN1MFAP5TGFB2TGFBR1TGFBR2About this report →
- Hereditary Arterial CalcificationReads 2 of these genesABCC6ENPP1About this report →
- NeurofibromatosisReads 2 of these genesLZTR1NF1About this report →
- Caffey DiseaseReads 1 of these genesCOL1A1About this report →
- Ferguson-Smith Disease (Multiple Self-Healing Squamous Epithelioma)Reads 1 of these genesTGFBR1About this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- Frank-Ter Haar SyndromeReads 1 of these genesSH3PXD2BAbout this report →
- H SyndromeReads 1 of these genesSLC29A3About this report →
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
- NEK8-Related Renal-Hepatic-Pancreatic DysplasiaReads 1 of these genesNEK8About this report →
- PLD1-Related Congenital Heart DiseaseReads 1 of these genesPLD1About this report →
- SF3B4-Related Acrofacial Dysostosis (Nager Syndrome)Reads 1 of these genesSF3B4About this report →
- Spondyloepiphyseal Dysplasia With Congenital Joint DislocationsReads 1 of these genesCHST3About this report →
- Turnpenny-Fry SyndromeReads 1 of these genesPCGF2About this report →
- Inherited Congenital Heart DefectsReads 3 of these genesTBX5ELNFLNAAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 4 of these genesBCORCOX7BHCCSNDUFB11About this report →
- Dilated CardiomyopathyReads 5 of these genesRAF1LMNAMYH7MYPNTTNAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 2 of these genesHCN4LMNAAbout this report →
- Hereditary Von Willebrand DiseaseReads 1 of these genesVWFAbout this report →
- Inherited ArthropathiesReads 1 of these genesPRG4About this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Pseudoxanthoma ElasticumReads 1 of these genesABCC6About this report →
- Sandhoff Disease and GM2 Activator DeficiencyReads 1 of these genesHEXBAbout this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL2A1XYLT1About this report →
- Myofibrillar MyopathiesReads 2 of these genesRYR1TTNAbout this report →
- Osteogenesis ImperfectaReads 3 of these genesXYLT2COL1A2COL1A1About this report →
- Congenital Disorders of GlycosylationReads 5 of these genesALG9B3GALT6CHST14B3GAT3DSEAbout this report →
- Cutis LaxaReads 2 of these genesELNATP6V1E1About this report →
- Achondrogenesis panelReads 1 of these genesCOL2A1About this report →
- GalactosemiaReads 1 of these genesGALEAbout this report →
- Distal MyopathiesReads 2 of these genesMYH7TTNAbout this report →
- Intellectual DisabilityReads 7 of these genesCREBBPEP300HNRNPH2ADNPFMN2MED12About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Hereditary SpherocytosisReads 1 of these genesANK1About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- VitreoretinopathyReads 2 of these genesXYLT2COL2A1About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Left Ventricular NoncompactionReads 1 of these genesMYH7About this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesENPP1About this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesLMNATTNAbout this report →
- Primary Mitochondrial DiseaseReads 4 of these genesDNAJC30POLGTWNKNDUFB11About this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Female InfertilityReads 2 of these genesTWNKFMR1About this report →
- Diamond-Blackfan AnemiaReads 1 of these genesRPL5About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesSACSTWNKAbout this report →
- Inherited Neurodegenerative DisordersReads 5 of these genesPOLGSACSTWNKFMR1HEXBAbout this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesCBSAbout this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesNEK8About this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesSKIAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesPOLGLMNAHEXBAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesROBO1About this report →
- Congenital Muscular DystrophiesReads 1 of these genesSELENONAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesGALEAbout this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Epilepsy (Full Panel)Reads 2 of these genesFLNAHNRNPH2About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesROBO1About this report →
- Other Inborn Errors of ImmunityReads 2 of these genesKRASNCF1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesHEXBAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Retinitis PigmentosaReads 1 of these genesIFT140About this report →
Lesen Sie die Gene aus, die mit Mitral valve prolapse zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
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Meinen Genome Test bestellen126 Gene mit Mitral valve prolapse verknüpft
Veränderungen in diesen Genen verursachen seltene Erkrankungen, bei denen Mitral valve prolapse 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 |
|---|---|---|
| AMOTL1angiomotin like 1 | Immer | In 1 Erkrankung |
| CREBBPCREB binding lysine acetyltransferase | Immer | In 1 Erkrankung |
| EP300EP300 lysine acetyltransferase | Immer | In 1 Erkrankung |
| FBN1fibrillin 1 | Immer | In 7 Erkrankungen |
| FIBPFGF1 intracellular binding protein | Immer | In 2 Erkrankungen |
| LZTR1leucine zipper like post translational regulator 1 | Immer | In 2 Erkrankungen |
| NR6A1nuclear receptor subfamily 6 group A member 1 | Immer | In 1 Erkrankung |
| RPS6KC1ribosomal protein S6 kinase C1 | Immer | In 1 Erkrankung |
| SF3B4splicing factor 3b subunit 4 | Immer | In 1 Erkrankung |
| TBX5T-box transcription factor 5 | Immer | In 1 Erkrankung |
| XYLT2xylosyltransferase 2 | Immer | In 2 Erkrankungen |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SH3PXD2BSH3 and PX domains 2B | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| AEBP1AE binding protein 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Häufig (30–79 %) | In 1 Erkrankung |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Häufig (30–79 %) | In 1 Erkrankung |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Häufig (30–79 %) | In 1 Erkrankung |
| CLIP2CAP-Gly domain containing linker protein 2 | Häufig (30–79 %) | In 1 Erkrankung |
| COL2A1collagen type II alpha 1 chain | Häufig (30–79 %) | In 2 Erkrankungen |
| COL3A1collagen type III alpha 1 chain | Häufig (30–79 %) | In 2 Erkrankungen |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Häufig (30–79 %) | In 1 Erkrankung |
| EIF4Heukaryotic translation initiation factor 4H | Häufig (30–79 %) | In 1 Erkrankung |
| ELNelastin | Häufig (30–79 %) | In 2 Erkrankungen |
| FBN2fibrillin 2 | Häufig (30–79 %) | In 2 Erkrankungen |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Häufig (30–79 %) | In 1 Erkrankung |
| FLNAfilamin A | Häufig (30–79 %) | In 4 Erkrankungen |
| GALEUDP-galactose-4-epimerase | Häufig (30–79 %) | In 1 Erkrankung |
| GTF2Igeneral transcription factor IIi | Häufig (30–79 %) | In 1 Erkrankung |
| GTF2IRD1GTF2I repeat domain containing 1 | Häufig (30–79 %) | In 1 Erkrankung |
| GTF2IRD2GTF2I repeat domain containing 2 | Häufig (30–79 %) | In 1 Erkrankung |
| HCN4hyperpolarization activated cyclic nucleotide gated potassium channel 4 | Häufig (30–79 %) | In 1 Erkrankung |
| HNRNPH2heterogeneous nuclear ribonucleoprotein H2 | Häufig (30–79 %) | In 1 Erkrankung |
| HRASHRas proto-oncogene, GTPase | Häufig (30–79 %) | In 2 Erkrankungen |
| KRASKRas proto-oncogene, GTPase | Häufig (30–79 %) | In 2 Erkrankungen |
| LIMK1LIM domain kinase 1 | Häufig (30–79 %) | In 1 Erkrankung |
| METTL27methyltransferase like 27 | Häufig (30–79 %) | In 1 Erkrankung |
| MLXIPLMLX interacting protein like | Häufig (30–79 %) | In 1 Erkrankung |
| NCF1neutrophil cytosolic factor 1 | Häufig (30–79 %) | In 1 Erkrankung |
| POLGDNA polymerase gamma, catalytic subunit | Häufig (30–79 %) | In 2 Erkrankungen |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Häufig (30–79 %) | In 2 Erkrankungen |
86 weitere Gene anzeigen
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Häufig (30–79 %) | In 1 Erkrankung |
| RFC2replication factor C subunit 2 | Häufig (30–79 %) | In 1 Erkrankung |
| RYR1ryanodine receptor 1 | Häufig (30–79 %) | In 1 Erkrankung |
| SACSsacsin molecular chaperone | Häufig (30–79 %) | In 1 Erkrankung |
| SKISKI proto-oncogene | Häufig (30–79 %) | In 2 Erkrankungen |
| STX1Asyntaxin 1A | Häufig (30–79 %) | In 1 Erkrankung |
| TBL2transducin beta like 2 | Häufig (30–79 %) | In 1 Erkrankung |
| TMEM270transmembrane protein 270 | Häufig (30–79 %) | In 1 Erkrankung |
| TWNKtwinkle mtDNA helicase | Häufig (30–79 %) | In 1 Erkrankung |
| VPS37DVPS37D subunit of ESCRT-I | Häufig (30–79 %) | In 1 Erkrankung |
| ABCC6ATP binding cassette subfamily C member 6 | Manchmal (5–29 %) | In 3 Erkrankungen |
| ADAMTS15ADAM metallopeptidase with thrombospondin type 1 motif 15 | Manchmal (5–29 %) | In 1 Erkrankung |
| ADNPactivity dependent neuroprotector homeobox | Manchmal (5–29 %) | In 1 Erkrankung |
| AGR2anterior gradient 2, protein disulphide isomerase family member | Manchmal (5–29 %) | In 1 Erkrankung |
| ALG5ALG5 dolichyl-phosphate beta-glucosyltransferase | Manchmal (5–29 %) | In 1 Erkrankung |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Manchmal (5–29 %) | In 1 Erkrankung |
| ANK1ankyrin 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| ATXN7L3ataxin 7 like 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| B3GALT6beta-1,3-galactosyltransferase 6 | Manchmal (5–29 %) | In 1 Erkrankung |
| BCORBCL6 corepressor | Manchmal (5–29 %) | In 2 Erkrankungen |
| BGNbiglycan | Manchmal (5–29 %) | In 1 Erkrankung |
| BICC1BicC family RNA binding protein 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| BRF1BRF1 general transcription factor IIIB subunit | Manchmal (5–29 %) | In 2 Erkrankungen |
| CHST14carbohydrate sulfotransferase 14 | Manchmal (5–29 %) | In 1 Erkrankung |
| CLIC2CLIC family member 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| COL1A2collagen type I alpha 2 chain | Manchmal (5–29 %) | In 2 Erkrankungen |
| COX7Bcytochrome c oxidase subunit 7B | Manchmal (5–29 %) | In 1 Erkrankung |
| DNAJB11DnaJ heat shock protein family (Hsp40) member B11 | Manchmal (5–29 %) | In 1 Erkrankung |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| EXTL3exostosin like glycosyltransferase 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| FMN2formin 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| FMR1fragile X messenger ribonucleoprotein 1 | Manchmal (5–29 %) | In 2 Erkrankungen |
| GANABglucosidase II alpha subunit | Manchmal (5–29 %) | In 1 Erkrankung |
| HCCSholocytochrome c synthase | Manchmal (5–29 %) | In 1 Erkrankung |
| IFT140intraflagellar transport 140 | Manchmal (5–29 %) | In 1 Erkrankung |
| IPO8importin 8 | Manchmal (5–29 %) | In 1 Erkrankung |
| LMNAlamin A/C | Manchmal (5–29 %) | In 1 Erkrankung |
| MAPK1mitogen-activated protein kinase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| MED12mediator complex subunit 12 | Manchmal (5–29 %) | In 1 Erkrankung |
| MFAP5microfibril associated protein 5 | Manchmal (5–29 %) | In 1 Erkrankung |
| MMP14matrix metallopeptidase 14 | Manchmal (5–29 %) | In 1 Erkrankung |
| MMP2matrix metallopeptidase 2 | Manchmal (5–29 %) | In 2 Erkrankungen |
| MYH7myosin heavy chain 7 | Manchmal (5–29 %) | In 1 Erkrankung |
| MYPNmyopalladin | Manchmal (5–29 %) | In 1 Erkrankung |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Manchmal (5–29 %) | In 1 Erkrankung |
| NEK8NIMA related kinase 8 | Manchmal (5–29 %) | In 1 Erkrankung |
| NPR3natriuretic peptide receptor 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| PKD1polycystin 1, transient receptor potential channel interacting | Manchmal (5–29 %) | In 2 Erkrankungen |
| PKD2polycystin 2, transient receptor potential cation channel | Manchmal (5–29 %) | In 1 Erkrankung |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| PRDM5PR/SET domain 5 | Manchmal (5–29 %) | In 1 Erkrankung |
| PRG4proteoglycan 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| ROBO1roundabout guidance receptor 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SELENONselenoprotein N | Manchmal (5–29 %) | In 1 Erkrankung |
| SLC29A3solute carrier family 29 member 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| SMAD3SMAD family member 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| SPRED2sprouty related EVH1 domain containing 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| TGFB2transforming growth factor beta 2 | Manchmal (5–29 %) | In 2 Erkrankungen |
| TGFBR1transforming growth factor beta receptor 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| TGFBR2transforming growth factor beta receptor 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| TNXBtenascin XB | Manchmal (5–29 %) | In 2 Erkrankungen |
| TPM2tropomyosin 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| TPM3tropomyosin 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| TTNtitin | Manchmal (5–29 %) | In 1 Erkrankung |
| VPS13Bvacuolar protein sorting 13 homolog B | Manchmal (5–29 %) | In 2 Erkrankungen |
| ZNF469zinc finger protein 469 | Manchmal (5–29 %) | In 2 Erkrankungen |
| COL1A1collagen type I alpha 1 chain | Selten (1–4 %) | In 2 Erkrankungen |
| COL5A1collagen type V alpha 1 chain | Selten (1–4 %) | In 2 Erkrankungen |
| COL5A2collagen type V alpha 2 chain | Selten (1–4 %) | In 1 Erkrankung |
| HEXBhexosaminidase subunit beta | Selten (1–4 %) | In 1 Erkrankung |
| NF1neurofibromin 1 | Selten (1–4 %) | In 1 Erkrankung |
| SPRED1sprouty related EVH1 domain containing 1 | Selten (1–4 %) | In 1 Erkrankung |
| XYLT1xylosyltransferase 1 | Selten (1–4 %) | In 1 Erkrankung |
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | Nicht erfasst | In 1 Erkrankung |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Nicht erfasst | In 1 Erkrankung |
| CBScystathionine beta-synthase | Nicht erfasst | In 1 Erkrankung |
| CHST3carbohydrate sulfotransferase 3 | Nicht erfasst | In 1 Erkrankung |
| DCHS1dachsous cadherin-related 1 | Nicht erfasst | In 1 Erkrankung |
| DSEdermatan sulfate epimerase | Nicht erfasst | In 1 Erkrankung |
| DZIP1DAZ interacting zinc finger protein 1 | Nicht erfasst | In 1 Erkrankung |
| LTBP3latent transforming growth factor beta binding protein 3 | Nicht erfasst | In 1 Erkrankung |
| PCGF2polycomb group ring finger 2 | Nicht erfasst | In 1 Erkrankung |
| PLD1phospholipase D1 | Nicht erfasst | In 1 Erkrankung |
| RPL5ribosomal protein L5 | Nicht erfasst | In 1 Erkrankung |
| SLC6A6solute carrier family 6 member 6 | Nicht erfasst | In 1 Erkrankung |
| VWFvon Willebrand factor | 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 2026.10.21-777c9289.
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