Tratto
Bleeding tendency
Nome clinico: 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.
Riepilogo
- Detto anche
- Bleeding diathesis, Hemorrhagic diathesis
- Sistema corporeo
- Abnormality of blood and blood-forming tissues
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Ottieni il mio 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 →
Leggi i geni collegati a Bleeding tendency e il resto del tuo genoma con un unico test.
A partire da 449 $Spedizione gratuita · Risultati in 6–8 settimane
Ottieni il mio Genome Test140 geni collegati a Bleeding tendency
Alterazioni in questi geni causano malattie rare in cui si osserva Bleeding tendency. La maggior parte delle persone con questo tratto non presenta nessuna di tali condizioni, e un gene di questo elenco non dice nulla sul genoma di nessuno in particolare.
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| ALG13ALG13 UDP-N-acetylglucosaminyltransferase subunit | Sempre | In 1 condizione |
| F13A1coagulation factor XIII A chain | Sempre | In 1 condizione |
| F13Bcoagulation factor XIII B chain | Sempre | In 1 condizione |
| FGAfibrinogen alpha chain | Sempre | In 4 condizioni |
| FGBfibrinogen beta chain | Sempre | In 4 condizioni |
| FGGfibrinogen gamma chain | Sempre | In 4 condizioni |
| FYB1FYN binding protein 1 | Sempre | In 1 condizione |
| GALEUDP-galactose-4-epimerase | Sempre | In 1 condizione |
| GFI1Bgrowth factor independent 1B transcriptional repressor | Sempre | In 1 condizione |
| HPS3HPS3 biogenesis of lysosomal organelles complex 2 subunit 1 | Sempre | In 1 condizione |
| HPS4HPS4 biogenesis of lysosomal organelles complex 3 subunit 2 | Sempre | In 1 condizione |
| ITGB3integrin subunit beta 3 | Sempre | In 3 condizioni |
| PRKACGprotein kinase cAMP-activated catalytic subunit gamma | Sempre | In 1 condizione |
| PTPRJprotein tyrosine phosphatase receptor type J | Sempre | In 1 condizione |
| ARF1ARF GTPase 1 | Molto spesso (80–99%) | In 1 condizione |
| ARFGEF2ARF guanine nucleotide exchange factor 2 | Molto spesso (80–99%) | In 1 condizione |
| BMPR1Abone morphogenetic protein receptor type 1A | Molto spesso (80–99%) | In 3 condizioni |
| CHST14carbohydrate sulfotransferase 14 | Molto spesso (80–99%) | In 1 condizione |
| DSEdermatan sulfate epimerase | Molto spesso (80–99%) | In 1 condizione |
| ENGendoglin | Molto spesso (80–99%) | In 1 condizione |
| ERMARDER membrane associated RNA degradation | Molto spesso (80–99%) | In 1 condizione |
| F11coagulation factor XI | Molto spesso (80–99%) | In 2 condizioni |
| F8coagulation factor VIII | Molto spesso (80–99%) | In 2 condizioni |
| FLNAfilamin A | Molto spesso (80–99%) | In 1 condizione |
| GATA1GATA binding protein 1 | Molto spesso (80–99%) | In 2 condizioni |
| GP1BAglycoprotein Ib platelet subunit alpha | Molto spesso (80–99%) | In 3 condizioni |
| GP1BBglycoprotein Ib platelet subunit beta | Molto spesso (80–99%) | In 3 condizioni |
| GP9glycoprotein IX platelet | Molto spesso (80–99%) | In 2 condizioni |
| GREM1gremlin 1, DAN family BMP antagonist | Molto spesso (80–99%) | In 1 condizione |
| JAK2Janus kinase 2 | Molto spesso (80–99%) | In 3 condizioni |
| MAP1Bmicrotubule associated protein 1B | Molto spesso (80–99%) | In 1 condizione |
| MPLMPL proto-oncogene, thrombopoietin receptor | Molto spesso (80–99%) | In 3 condizioni |
| NBEAL2neurobeachin like 2 | Molto spesso (80–99%) | In 2 condizioni |
| NEDD4LNEDD4 like E3 ubiquitin protein ligase | Molto spesso (80–99%) | In 1 condizione |
| SLC35A1solute carrier family 35 member A1 | Molto spesso (80–99%) | In 1 condizione |
| SMAD4SMAD family member 4 | Molto spesso (80–99%) | In 1 condizione |
| THPOthrombopoietin | Molto spesso (80–99%) | In 2 condizioni |
| TMTC3transmembrane O-mannosyltransferase targeting cadherins 3 | Molto spesso (80–99%) | In 1 condizione |
| ATRXATRX chromatin remodeler | Spesso (30–79%) | In 1 condizione |
| BCORBCL6 corepressor | Spesso (30–79%) | In 1 condizione |
Mostra altri 100 geni
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Spesso (30–79%) | In 2 condizioni |
| CALRcalreticulin | Spesso (30–79%) | In 2 condizioni |
| CASP10caspase 10 | Spesso (30–79%) | In 1 condizione |
| CBLCbl proto-oncogene | Spesso (30–79%) | In 1 condizione |
| CD109CD109 molecule | Spesso (30–79%) | In 1 condizione |
| F2coagulation factor II, thrombin | Spesso (30–79%) | In 1 condizione |
| FASFas cell surface death receptor | Spesso (30–79%) | In 1 condizione |
| FASLGFas ligand | Spesso (30–79%) | In 1 condizione |
| FIP1L1factor interacting with PAPOLA and CPSF1 | Spesso (30–79%) | In 1 condizione |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Spesso (30–79%) | In 2 condizioni |
| GGCXgamma-glutamyl carboxylase | Spesso (30–79%) | In 4 condizioni |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | Spesso (30–79%) | In 1 condizione |
| ITGA2integrin subunit alpha 2 | Spesso (30–79%) | In 1 condizione |
| ITGA2Bintegrin subunit alpha 2b | Spesso (30–79%) | In 2 condizioni |
| KRASKRas proto-oncogene, GTPase | Spesso (30–79%) | In 1 condizione |
| LYSTlysosomal trafficking regulator | Spesso (30–79%) | In 1 condizione |
| LZTR1leucine zipper like post translational regulator 1 | Spesso (30–79%) | In 1 condizione |
| MRASmuscle RAS oncogene homolog | Spesso (30–79%) | In 1 condizione |
| NABP1nucleic acid binding protein 1 | Spesso (30–79%) | In 1 condizione |
| NPM1nucleophosmin 1 | Spesso (30–79%) | In 1 condizione |
| NRASNRAS proto-oncogene, GTPase | Spesso (30–79%) | In 1 condizione |
| NUMA1nuclear mitotic apparatus protein 1 | Spesso (30–79%) | In 1 condizione |
| PMLPML nuclear body scaffold | Spesso (30–79%) | In 1 condizione |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Spesso (30–79%) | In 1 condizione |
| PTENphosphatase and tensin homolog | Spesso (30–79%) | In 1 condizione |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Spesso (30–79%) | In 2 condizioni |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Spesso (30–79%) | In 1 condizione |
| RARAretinoic acid receptor alpha | Spesso (30–79%) | In 1 condizione |
| RASA2RAS p21 protein activator 2 | Spesso (30–79%) | In 1 condizione |
| RFT1RFT1 glycolipid translocator homolog | Spesso (30–79%) | In 1 condizione |
| RIT1Ras like without CAAX 1 | Spesso (30–79%) | In 1 condizione |
| RRASRAS related | Spesso (30–79%) | In 1 condizione |
| RRAS2RAS related 2 | Spesso (30–79%) | In 1 condizione |
| SERPINF2serpin family F member 2 | Spesso (30–79%) | In 1 condizione |
| SH2B3SH2B adaptor protein 3 | Spesso (30–79%) | In 1 condizione |
| SLC7A7solute carrier family 7 member 7 | Spesso (30–79%) | In 1 condizione |
| SOS1SOS Ras/Rac guanine nucleotide exchange factor 1 | Spesso (30–79%) | In 2 condizioni |
| SOS2SOS Ras/Rho guanine nucleotide exchange factor 2 | Spesso (30–79%) | In 1 condizione |
| SPRED2sprouty related EVH1 domain containing 2 | Spesso (30–79%) | In 1 condizione |
| STAT3signal transducer and activator of transcription 3 | Spesso (30–79%) | In 1 condizione |
| STAT5Bsignal transducer and activator of transcription 5B | Spesso (30–79%) | In 1 condizione |
| TBL1XR1TBL1X/Y related 1 | Spesso (30–79%) | In 1 condizione |
| TET2tet methylcytosine dioxygenase 2 | Spesso (30–79%) | In 4 condizioni |
| TP53tumor protein p53 | Spesso (30–79%) | In 1 condizione |
| VKORC1vitamin K epoxide reductase complex subunit 1 | Spesso (30–79%) | In 2 condizioni |
| ZBTB16zinc finger and BTB domain containing 16 | Spesso (30–79%) | In 1 condizione |
| ALKALK receptor tyrosine kinase | A volte (5–29%) | In 1 condizione |
| AMNamnion associated transmembrane protein | A volte (5–29%) | In 1 condizione |
| B4GALT1beta-1,4-galactosyltransferase 1 | A volte (5–29%) | In 1 condizione |
| CLPBClpB family mitochondrial disaggregase | A volte (5–29%) | In 1 condizione |
| COG6component of oligomeric golgi complex 6 | A volte (5–29%) | In 1 condizione |
| CUBNcubilin | A volte (5–29%) | In 1 condizione |
| EPORerythropoietin receptor | A volte (5–29%) | In 1 condizione |
| GBA1glucosylceramidase beta 1 | A volte (5–29%) | In 1 condizione |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | A volte (5–29%) | In 1 condizione |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | A volte (5–29%) | In 1 condizione |
| IPO8importin 8 | A volte (5–29%) | In 1 condizione |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | A volte (5–29%) | In 1 condizione |
| LMO1LIM domain only 1 | A volte (5–29%) | In 1 condizione |
| MAP2K1mitogen-activated protein kinase kinase 1 | A volte (5–29%) | In 1 condizione |
| MGAT2alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | A volte (5–29%) | In 1 condizione |
| MYCNMYCN proto-oncogene, bHLH transcription factor | A volte (5–29%) | In 1 condizione |
| PHOX2Bpaired like homeobox 2B | A volte (5–29%) | In 1 condizione |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | A volte (5–29%) | In 1 condizione |
| RASA1RAS p21 protein activator 1 | A volte (5–29%) | In 1 condizione |
| RPS14ribosomal protein S14 | A volte (5–29%) | In 1 condizione |
| RYR1ryanodine receptor 1 | A volte (5–29%) | In 1 condizione |
| SCARB2scavenger receptor class B member 2 | A volte (5–29%) | In 1 condizione |
| SLC37A4solute carrier family 37 member 4 | A volte (5–29%) | In 1 condizione |
| SMAD2SMAD family member 2 | A volte (5–29%) | In 1 condizione |
| SMAD3SMAD family member 3 | A volte (5–29%) | In 1 condizione |
| TGFB2transforming growth factor beta 2 | A volte (5–29%) | In 1 condizione |
| TGFB3transforming growth factor beta 3 | A volte (5–29%) | In 1 condizione |
| TGFBR1transforming growth factor beta receptor 1 | A volte (5–29%) | In 1 condizione |
| TGFBR2transforming growth factor beta receptor 2 | A volte (5–29%) | In 1 condizione |
| URODuroporphyrinogen decarboxylase | A volte (5–29%) | In 1 condizione |
| UROSuroporphyrinogen III synthase | A volte (5–29%) | In 1 condizione |
| VPS33BVPS33B late endosome and lysosome associated | A volte (5–29%) | In 1 condizione |
| F12coagulation factor XII | Raramente (1–4%) | In 1 condizione |
| MTTPmicrosomal triglyceride transfer protein | Raramente (1–4%) | In 1 condizione |
| SF3B1splicing factor 3b subunit 1 | Raramente (1–4%) | In 1 condizione |
| SLC25A13solute carrier family 25 member 13 | Raramente (1–4%) | In 1 condizione |
| SMPD1sphingomyelin phosphodiesterase 1 | Raramente (1–4%) | In 1 condizione |
| ABCG8ATP binding cassette subfamily G member 8 | Non registrato | In 1 condizione |
| ANO6anoctamin 6 | Non registrato | In 1 condizione |
| CD36CD36 molecule (CD36 blood group) | Non registrato | In 1 condizione |
| CISD2CDGSH iron sulfur domain 2 | Non registrato | In 1 condizione |
| F5coagulation factor V | Non registrato | In 1 condizione |
| F7coagulation factor VII | Non registrato | In 1 condizione |
| FERMT3FERM domain containing kindlin 3 | Non registrato | In 1 condizione |
| G6PC1glucose-6-phosphatase catalytic subunit 1 | Non registrato | In 1 condizione |
| LMAN1lectin, mannose binding 1 | Non registrato | In 1 condizione |
| MPImannose phosphate isomerase | Non registrato | In 1 condizione |
| MYH9myosin heavy chain 9 | Non registrato | In 1 condizione |
| P2RY12purinergic receptor P2Y12 | Non registrato | In 1 condizione |
| PEX12peroxisomal biogenesis factor 12 | Non registrato | In 1 condizione |
| SERPINE1serpin family E member 1 | Non registrato | In 1 condizione |
| SRCSRC proto-oncogene, non-receptor tyrosine kinase | Non registrato | In 1 condizione |
| STIM1stromal interaction molecule 1 | Non registrato | In 1 condizione |
| VWFvon Willebrand factor | Non registrato | In 1 condizione |
Con quale frequenza questo tratto si presenta tra le persone con una delle condizioni legate al gene, nella misura più alta riscontrata tra queste, secondo quanto registrato dall'Human Phenotype Ontology. Queste pagine descrivono tratti e la ricerca che li riguarda; non costituiscono una diagnosi, e per i sintomi il medico o il consulente genetico è la persona a cui rivolgersi.
Tratti più specifici
- Bloody nose110 geni
- Bleeding gums61 geni
- Prolonged bleeding time48 geni
- Abnormally heavy bleeding during menstruation43 geni
- Oral cavity bleeding22 geni
- Bleeding below the skin15 geni
- Excessive bleeding after minor trauma15 geni
- Cephalohematoma13 geni
- Internal bleeding11 geni
- Abnormal umbilical stump bleeding10 geni
- Bleeding with minor or no trauma8 geni
- Prolonged bleeding following procedure7 geni
- Excessive bleeding from superficial cuts5 geni
- Abnormal vaginal bleeding2 geni
- Bleeding requiring red cell transfusion1 gene
- Excessive bleeding after a venipuncture1 gene
- Abnormal onset of bleeding
Tratti più generali
Fonte dei dati
- Human Phenotype Ontology, versione 2026-09-01: il tratto, i suoi nomi, la sua definizione e i geni a esso collegati. Per saperne di più visiti hpo.jax.org.
- Versione dei dati 2026.10.18-8b139e39.
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