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Træk
Bleeding tendency
Klinisk navn: Abnormal bleeding
An abnormal susceptibility to bleeding, often referred to as a bleeding diathesis. A bleeding diathesis may be related to vascular, platelet and coagulation defects.
Resumé
- Også kaldet
- Bleeding diathesis, Hemorrhagic diathesis
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Denne 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/abnormal-bleeding.json"
page <- fromJSON(url)
page$trait$nameBleeding tendencyHP:0001892
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Læs de gener, der er knyttet til Bleeding tendency, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test94 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.
- Noonan SyndromeReads 15 of these genesBRAFCBLKRASLZTR1MRASNRASAbout this report →
- Rare Inherited Coagulation Factor DeficienciesReads 8 of these genesF13A1F13BF2GGCXVKORC1F5About this report →
- Loeys-Dietz SyndromeReads 6 of these genesSMAD2SMAD3TGFB2TGFB3TGFBR1TGFBR2About this report →
- Inherited Platelet Function DisordersReads 7 of these genesITGB3GP1BAGP1BBGP9NBEAL2ITGA2BAbout this report →
Show 90 more reports
- Periventricular Nodular HeterotopiaReads 5 of these genesARF1ARFGEF2FLNAMAP1BNEDD4LAbout this report →
- Inherited ThrombocytopeniasReads 12 of these genesFYB1GALEGFI1BGATA1GP1BBMPLAbout this report →
- Marfan Like SyndromesReads 6 of these genesSMAD2SMAD3TGFB2TGFB3TGFBR1TGFBR2About this report →
- Hypertrophic CardiomyopathyReads 14 of these genesBRAFKRASLZTR1MRASNRASPTPN11About this report →
- Congenital AfibrinogenemiaReads 3 of these genesFGAFGBFGGAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 4 of these genesCASP10FASFASLGKRASAbout this report →
- Hereditary Mixed Polyposis SyndromeReads 2 of these genesBMPR1AGREM1About this report →
- Hereditary Von Willebrand DiseaseReads 2 of these genesGP1BAVWFAbout this report →
- ITGA2B/ITGB3-Related MacrothrombocytopeniaReads 2 of these genesITGB3ITGA2BAbout this report →
- Juvenile Polyposis SyndromeReads 2 of these genesBMPR1ASMAD4About this report →
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 2 of these genesALKPHOX2BAbout this report →
- HaemophiliaReads 2 of these genesF11F8About this report →
- Autoimmune DiseaseReads 5 of these genesCASP10FASFASLGKRASSTAT3About this report →
- Congenital Disorders of GlycosylationReads 10 of these genesALG13CHST14DSESLC35A1RFT1B4GALT1About this report →
- Hereditary Hemorrhagic TelangiectasiaReads 2 of these genesENGSMAD4About this report →
- Inherited Fibrinolytic DisordersReads 2 of these genesSERPINF2SERPINE1About this report →
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
- ARC Syndrome 1 (VPS33B)Reads 1 of these genesVPS33BAbout this report →
- Chediak-Higashi syndromeReads 1 of these genesLYSTAbout this report →
- Congenital Bile Acid Synthesis Defect 1 (HSD3B7)Reads 1 of these genesHSD3B7About this report →
- Congenital Central Hypoventilation SyndromeReads 1 of these genesPHOX2BAbout this report →
- Congenital Factor XII DeficiencyReads 1 of these genesF12About this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- Ferguson-Smith Disease (Multiple Self-Healing Squamous Epithelioma)Reads 1 of these genesTGFBR1About this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- Hereditary Thrombocythaemia (JAK2)Reads 1 of these genesJAK2About this report →
- Hereditary Thrombocythaemia (THPO)Reads 1 of these genesTHPOAbout this report →
- ITGB3-Related MacrothrombocytopeniaReads 1 of these genesITGB3About this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- MPL-Related Hereditary ThrombocythaemiaReads 1 of these genesMPLAbout this report →
- SH2B3-Related Immune DysregulationReads 1 of these genesSH2B3About this report →
- Aortic AneurysmReads 3 of these genesTGFB2TGFBR1TGFBR2About this report →
- CitrullinemiaReads 1 of these genesSLC25A13About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- Hereditary Gingival FibromatosisReads 1 of these genesSOS1About this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Pseudoxanthoma ElasticumReads 1 of these genesGGCXAbout this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- Tubular Aggregate MyopathyReads 1 of these genesSTIM1About this report →
- Wolfram Syndrome & WFS1 SpectrumReads 1 of these genesCISD2About this report →
- PorphyriaReads 2 of these genesURODUROSAbout this report →
- ThrombophiliaReads 2 of these genesF2F5About this report →
- Ehlers-Danlos SyndromeReads 3 of these genesCHST14DSEPLOD1About this report →
- Other Inborn Errors of ImmunityReads 9 of these genesCASP10FASFASLGIRF2BP2KRASLYSTAbout this report →
- Hermansky-Pudlak SyndromeReads 2 of these genesHPS3HPS4About this report →
- Urea Cycle DisorderReads 2 of these genesSLC7A7SLC25A13About this report →
- Hereditary AngioedemaReads 1 of these genesF12About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesPHOX2BAbout this report →
- Leukocyte Adhesion DeficiencyReads 1 of these genesFERMT3About this report →
- Glycogen Storage DiseaseReads 2 of these genesSLC37A4G6PC1About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- GalactosemiaReads 1 of these genesGALEAbout this report →
- Hereditary Vascular MalformationsReads 1 of these genesRASA1About this report →
- NeurofibromatosisReads 1 of these genesLZTR1About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesPRKAR1AAbout this report →
- Homocystinuria & Cobalamin DisordersReads 2 of these genesAMNCUBNAbout this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesSTAT5BAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Hereditary HypolipoproteinemiasReads 1 of these genesMTTPAbout this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT3About this report →
- Hepatic Porphyria DisordersReads 1 of these genesURODAbout this report →
- Malignant Endocrine NeoplasmReads 1 of these genesTP53About this report →
- PolycythemiaReads 1 of these genesEPORAbout this report →
- Kidney CancerReads 1 of these genesTP53About this report →
- Rare Hereditary Peripheral NeuropathiesReads 5 of these genesFGALYSTMTTPSMPD1PEX12About this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 1 of these genesIRF2BP2About this report →
- Epilepsy (Full Panel)Reads 4 of these genesALG13FLNAHACE1SCARB2About this report →
- Hereditary AmyloidosisReads 1 of these genesFGAAbout this report →
- Severe Congenital NeutropeniaReads 1 of these genesCLPBAbout this report →
- Urinary and Renal System TumourReads 1 of these genesTP53About this report →
- HyperlipidemiaReads 1 of these genesABCG8About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesRYR1About this report →
- Diamond-Blackfan AnemiaReads 1 of these genesGATA1About this report →
- OsteopetrosisReads 1 of these genesFERMT3About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX12About this report →
- Lysosomal Storage DiseaseReads 2 of these genesGBA1SMPD1About this report →
- Parkinson DiseaseReads 1 of these genesGBA1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Congenital MyopathiesReads 1 of these genesRYR1About this report →
- Dyskeratosis CongenitaReads 1 of these genesNPM1About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesTMTC3About this report →
- Inherited Neurodegenerative DisordersReads 4 of these genesLYSTHACE1MTTPPEX12About this report →
- Hearing Loss and DeafnessReads 2 of these genesMAP1BMYH9About this report →
- Intellectual DisabilityReads 3 of these genesSMAD4ATRXTBL1XR1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Dilated CardiomyopathyReads 1 of these genesRAF1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesMTTPAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesHACE1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPEX12About this report →
Læs de gener, der er knyttet til Bleeding tendency, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test140 gener knyttet til Bleeding tendency
Ændringer i disse gener forårsager sjældne tilstande, hvor Bleeding tendency 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 |
|---|---|---|
| ALG13ALG13 UDP-N-acetylglucosaminyltransferase subunit | Altid | I 1 tilstand |
| F13A1coagulation factor XIII A chain | Altid | I 1 tilstand |
| F13Bcoagulation factor XIII B chain | Altid | I 1 tilstand |
| FGAfibrinogen alpha chain | Altid | I 4 tilstande |
| FGBfibrinogen beta chain | Altid | I 4 tilstande |
| FGGfibrinogen gamma chain | Altid | I 4 tilstande |
| FYB1FYN binding protein 1 | Altid | I 1 tilstand |
| GALEUDP-galactose-4-epimerase | Altid | I 1 tilstand |
| GFI1Bgrowth factor independent 1B transcriptional repressor | Altid | I 1 tilstand |
| HPS3HPS3 biogenesis of lysosomal organelles complex 2 subunit 1 | Altid | I 1 tilstand |
| HPS4HPS4 biogenesis of lysosomal organelles complex 3 subunit 2 | Altid | I 1 tilstand |
| ITGB3integrin subunit beta 3 | Altid | I 3 tilstande |
| PRKACGprotein kinase cAMP-activated catalytic subunit gamma | Altid | I 1 tilstand |
| PTPRJprotein tyrosine phosphatase receptor type J | Altid | I 1 tilstand |
| ARF1ARF GTPase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| ARFGEF2ARF guanine nucleotide exchange factor 2 | Meget ofte (80–99 %) | I 1 tilstand |
| BMPR1Abone morphogenetic protein receptor type 1A | Meget ofte (80–99 %) | I 3 tilstande |
| CHST14carbohydrate sulfotransferase 14 | Meget ofte (80–99 %) | I 1 tilstand |
| DSEdermatan sulfate epimerase | Meget ofte (80–99 %) | I 1 tilstand |
| ENGendoglin | Meget ofte (80–99 %) | I 1 tilstand |
| ERMARDER membrane associated RNA degradation | Meget ofte (80–99 %) | I 1 tilstand |
| F11coagulation factor XI | Meget ofte (80–99 %) | I 2 tilstande |
| F8coagulation factor VIII | Meget ofte (80–99 %) | I 2 tilstande |
| FLNAfilamin A | Meget ofte (80–99 %) | I 1 tilstand |
| GATA1GATA binding protein 1 | Meget ofte (80–99 %) | I 2 tilstande |
| GP1BAglycoprotein Ib platelet subunit alpha | Meget ofte (80–99 %) | I 3 tilstande |
| GP1BBglycoprotein Ib platelet subunit beta | Meget ofte (80–99 %) | I 3 tilstande |
| GP9glycoprotein IX platelet | Meget ofte (80–99 %) | I 2 tilstande |
| GREM1gremlin 1, DAN family BMP antagonist | Meget ofte (80–99 %) | I 1 tilstand |
| JAK2Janus kinase 2 | Meget ofte (80–99 %) | I 3 tilstande |
| MAP1Bmicrotubule associated protein 1B | Meget ofte (80–99 %) | I 1 tilstand |
| MPLMPL proto-oncogene, thrombopoietin receptor | Meget ofte (80–99 %) | I 3 tilstande |
| NBEAL2neurobeachin like 2 | Meget ofte (80–99 %) | I 2 tilstande |
| NEDD4LNEDD4 like E3 ubiquitin protein ligase | Meget ofte (80–99 %) | I 1 tilstand |
| SLC35A1solute carrier family 35 member A1 | Meget ofte (80–99 %) | I 1 tilstand |
| SMAD4SMAD family member 4 | Meget ofte (80–99 %) | I 1 tilstand |
| THPOthrombopoietin | Meget ofte (80–99 %) | I 2 tilstande |
| TMTC3transmembrane O-mannosyltransferase targeting cadherins 3 | Meget ofte (80–99 %) | I 1 tilstand |
| ATRXATRX chromatin remodeler | Ofte (30–79 %) | I 1 tilstand |
| BCORBCL6 corepressor | Ofte (30–79 %) | I 1 tilstand |
Vis 100 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Ofte (30–79 %) | I 2 tilstande |
| CALRcalreticulin | Ofte (30–79 %) | I 2 tilstande |
| CASP10caspase 10 | Ofte (30–79 %) | I 1 tilstand |
| CBLCbl proto-oncogene | Ofte (30–79 %) | I 1 tilstand |
| CD109CD109 molecule | Ofte (30–79 %) | I 1 tilstand |
| F2coagulation factor II, thrombin | Ofte (30–79 %) | I 1 tilstand |
| FASFas cell surface death receptor | Ofte (30–79 %) | I 1 tilstand |
| FASLGFas ligand | Ofte (30–79 %) | I 1 tilstand |
| FIP1L1factor interacting with PAPOLA and CPSF1 | Ofte (30–79 %) | I 1 tilstand |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Ofte (30–79 %) | I 2 tilstande |
| GGCXgamma-glutamyl carboxylase | Ofte (30–79 %) | I 4 tilstande |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | Ofte (30–79 %) | I 1 tilstand |
| ITGA2integrin subunit alpha 2 | Ofte (30–79 %) | I 1 tilstand |
| ITGA2Bintegrin subunit alpha 2b | Ofte (30–79 %) | I 2 tilstande |
| KRASKRas proto-oncogene, GTPase | Ofte (30–79 %) | I 1 tilstand |
| LYSTlysosomal trafficking regulator | Ofte (30–79 %) | I 1 tilstand |
| LZTR1leucine zipper like post translational regulator 1 | Ofte (30–79 %) | I 1 tilstand |
| MRASmuscle RAS oncogene homolog | Ofte (30–79 %) | I 1 tilstand |
| NABP1nucleic acid binding protein 1 | Ofte (30–79 %) | I 1 tilstand |
| NPM1nucleophosmin 1 | Ofte (30–79 %) | I 1 tilstand |
| NRASNRAS proto-oncogene, GTPase | Ofte (30–79 %) | I 1 tilstand |
| NUMA1nuclear mitotic apparatus protein 1 | Ofte (30–79 %) | I 1 tilstand |
| PMLPML nuclear body scaffold | Ofte (30–79 %) | I 1 tilstand |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| PTENphosphatase and tensin homolog | Ofte (30–79 %) | I 1 tilstand |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Ofte (30–79 %) | I 2 tilstande |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Ofte (30–79 %) | I 1 tilstand |
| RARAretinoic acid receptor alpha | Ofte (30–79 %) | I 1 tilstand |
| RASA2RAS p21 protein activator 2 | Ofte (30–79 %) | I 1 tilstand |
| RFT1RFT1 glycolipid translocator homolog | Ofte (30–79 %) | I 1 tilstand |
| RIT1Ras like without CAAX 1 | Ofte (30–79 %) | I 1 tilstand |
| RRASRAS related | Ofte (30–79 %) | I 1 tilstand |
| RRAS2RAS related 2 | Ofte (30–79 %) | I 1 tilstand |
| SERPINF2serpin family F member 2 | Ofte (30–79 %) | I 1 tilstand |
| SH2B3SH2B adaptor protein 3 | Ofte (30–79 %) | I 1 tilstand |
| SLC7A7solute carrier family 7 member 7 | Ofte (30–79 %) | I 1 tilstand |
| SOS1SOS Ras/Rac guanine nucleotide exchange factor 1 | Ofte (30–79 %) | I 2 tilstande |
| SOS2SOS Ras/Rho guanine nucleotide exchange factor 2 | Ofte (30–79 %) | I 1 tilstand |
| SPRED2sprouty related EVH1 domain containing 2 | Ofte (30–79 %) | I 1 tilstand |
| STAT3signal transducer and activator of transcription 3 | Ofte (30–79 %) | I 1 tilstand |
| STAT5Bsignal transducer and activator of transcription 5B | Ofte (30–79 %) | I 1 tilstand |
| TBL1XR1TBL1X/Y related 1 | Ofte (30–79 %) | I 1 tilstand |
| TET2tet methylcytosine dioxygenase 2 | Ofte (30–79 %) | I 4 tilstande |
| TP53tumor protein p53 | Ofte (30–79 %) | I 1 tilstand |
| VKORC1vitamin K epoxide reductase complex subunit 1 | Ofte (30–79 %) | I 2 tilstande |
| ZBTB16zinc finger and BTB domain containing 16 | Ofte (30–79 %) | I 1 tilstand |
| ALKALK receptor tyrosine kinase | Nogle gange (5–29 %) | I 1 tilstand |
| AMNamnion associated transmembrane protein | Nogle gange (5–29 %) | I 1 tilstand |
| B4GALT1beta-1,4-galactosyltransferase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CLPBClpB family mitochondrial disaggregase | Nogle gange (5–29 %) | I 1 tilstand |
| COG6component of oligomeric golgi complex 6 | Nogle gange (5–29 %) | I 1 tilstand |
| CUBNcubilin | Nogle gange (5–29 %) | I 1 tilstand |
| EPORerythropoietin receptor | Nogle gange (5–29 %) | I 1 tilstand |
| GBA1glucosylceramidase beta 1 | Nogle gange (5–29 %) | I 1 tilstand |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Nogle gange (5–29 %) | I 1 tilstand |
| IPO8importin 8 | Nogle gange (5–29 %) | I 1 tilstand |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | Nogle gange (5–29 %) | I 1 tilstand |
| LMO1LIM domain only 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MAP2K1mitogen-activated protein kinase kinase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MGAT2alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Nogle gange (5–29 %) | I 1 tilstand |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Nogle gange (5–29 %) | I 1 tilstand |
| PHOX2Bpaired like homeobox 2B | Nogle gange (5–29 %) | I 1 tilstand |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RASA1RAS p21 protein activator 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS14ribosomal protein S14 | Nogle gange (5–29 %) | I 1 tilstand |
| RYR1ryanodine receptor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SCARB2scavenger receptor class B member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC37A4solute carrier family 37 member 4 | Nogle gange (5–29 %) | I 1 tilstand |
| SMAD2SMAD family member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SMAD3SMAD family member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| TGFB2transforming growth factor beta 2 | Nogle gange (5–29 %) | I 1 tilstand |
| TGFB3transforming growth factor beta 3 | Nogle gange (5–29 %) | I 1 tilstand |
| TGFBR1transforming growth factor beta receptor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TGFBR2transforming growth factor beta receptor 2 | Nogle gange (5–29 %) | I 1 tilstand |
| URODuroporphyrinogen decarboxylase | Nogle gange (5–29 %) | I 1 tilstand |
| UROSuroporphyrinogen III synthase | Nogle gange (5–29 %) | I 1 tilstand |
| VPS33BVPS33B late endosome and lysosome associated | Nogle gange (5–29 %) | I 1 tilstand |
| F12coagulation factor XII | Sjældent (1–4%) | I 1 tilstand |
| MTTPmicrosomal triglyceride transfer protein | Sjældent (1–4%) | I 1 tilstand |
| SF3B1splicing factor 3b subunit 1 | Sjældent (1–4%) | I 1 tilstand |
| SLC25A13solute carrier family 25 member 13 | Sjældent (1–4%) | I 1 tilstand |
| SMPD1sphingomyelin phosphodiesterase 1 | Sjældent (1–4%) | I 1 tilstand |
| ABCG8ATP binding cassette subfamily G member 8 | Ikke registreret | I 1 tilstand |
| ANO6anoctamin 6 | Ikke registreret | I 1 tilstand |
| CD36CD36 molecule (CD36 blood group) | Ikke registreret | I 1 tilstand |
| CISD2CDGSH iron sulfur domain 2 | Ikke registreret | I 1 tilstand |
| F5coagulation factor V | Ikke registreret | I 1 tilstand |
| F7coagulation factor VII | Ikke registreret | I 1 tilstand |
| FERMT3FERM domain containing kindlin 3 | Ikke registreret | I 1 tilstand |
| G6PC1glucose-6-phosphatase catalytic subunit 1 | Ikke registreret | I 1 tilstand |
| LMAN1lectin, mannose binding 1 | Ikke registreret | I 1 tilstand |
| MPImannose phosphate isomerase | Ikke registreret | I 1 tilstand |
| MYH9myosin heavy chain 9 | Ikke registreret | I 1 tilstand |
| P2RY12purinergic receptor P2Y12 | Ikke registreret | I 1 tilstand |
| PEX12peroxisomal biogenesis factor 12 | Ikke registreret | I 1 tilstand |
| SERPINE1serpin family E member 1 | Ikke registreret | I 1 tilstand |
| SRCSRC proto-oncogene, non-receptor tyrosine kinase | Ikke registreret | I 1 tilstand |
| STIM1stromal interaction molecule 1 | Ikke registreret | I 1 tilstand |
| VWFvon Willebrand factor | 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.
Snævrere træk
- Bloody nose110 gener
- Bleeding gums61 gener
- Prolonged bleeding time48 gener
- Abnormally heavy bleeding during menstruation43 gener
- Oral cavity bleeding22 gener
- Bleeding below the skin15 gener
- Excessive bleeding after minor trauma15 gener
- Cephalohematoma13 gener
- Internal bleeding11 gener
- Abnormal umbilical stump bleeding10 gener
- Bleeding with minor or no trauma8 gener
- Prolonged bleeding following procedure7 gener
- Excessive bleeding from superficial cuts5 gener
- Abnormal vaginal bleeding2 gener
- Bleeding requiring red cell transfusion1 gen
- Excessive bleeding after a venipuncture1 gen
- Abnormal onset of bleeding
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 2026.10.18-8b139e39.
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