Combined Deficiency Of Factor V And Factor VIII
Combined Deficiency Of Factor V And Factor VIII
About the Disease
Factor V and Factor Viii, Combined Deficiency of, 2, also known as factor v and factor viii, combined deficiency of, is related to factor v and factor viii, combined deficiency of, 1 and hereditary combined deficiency of vitamin k-dependent clotting factors. An important gene associated with Factor V and Factor Viii, Combined Deficiency of, 2 is MCFD2 (Multiple Coagulation Factor Deficiency 2, ER Cargo Receptor Complex Subunit), and among its related pathways/superpathways are Metabolism of proteins and Vesicle-mediated transport. Affiliated tissues include bone marrow, bone and testis, and related phenotypes are prolonged prothrombin time and prolonged partial thromboplastin time
Common Targets
LMAN1 | MCFD2 | F11
Note: If you'd like to get a target analysis report for Combined Deficiency Of Factor V And Factor VIII, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Combined Deficiency Of Factor V And Factor VIII at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.
Other Diseases
Hermansky-Pudlak Syndrome | Astrocytoma | PHARC Syndrome | Kindler Syndrome | Hyperglycemia | Pitt-Hopkins Syndrome | Bronchiolitis | Chondroma | Duchenne Muscular Dystrophy | Congenital Bilateral Absence Of Vas Deferens | Cardiomyopathy, Hypertrophic | Acrodermatitis | Aspergillosis | Arterial Tortuosity Syndrome | Prurigo Nodularis | Stomatitis | Uterine Leiomyoma | Atelosteogenesis Type 2 | Hereditary Xerocytosis | Liddle Syndrome | Hyperlipidemia, Familial Combined | Myositis, Focal | Bartsocas-Papas Syndrome | Niemann-Pick Disease, Type B | Strabismus | McLeod Syndrome | Early Infantile Epileptic Encephalopathy 28 | Infectious Diarrhea | Celiac Disease | Pelvic Inflammatory Disease | Spinal Muscular Atrophy | Dementia | Pleomorphic Xanthoastrocytoma | Meningeal Melanocytoma | Presbyopia | Osteopetrosis | Reticular Dysgenesis | Galactosemia | Epiphyseal Chondrodysplasia, Miura Type | Prader-Willi Syndrome | Congenital Hereditary Endothelial Dystrophy Type II | Osteogenesis Imperfecta Type I | Smoldering Myeloma | Mitochondrial DNA Depletion Syndrome 13 | Acrocallosal Syndrome | Sensorineural Hearing Loss | Fibrosis | Fontaine Progeroid Syndrome | Ichthyosis, X-linked | Lateral Meningocele Syndrome | Pleural Tuberculosis | Thalassemia, Beta | Otopalatodigital Syndrome Type 2 | Dyslexia | Lafora Disease | Hypopigmentation | Weill-Marchesani Syndrome | Lennox-Gastaut Syndrome | Stickler Syndrome | Adenocarcinoma | Lymphoma Lymphoblastic | Obesity | Bladder Exstrophy | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Gallstones | Greig Cephalopolysyndactyly Syndrome | Pneumonia, Bacterial | Vertigo | Atopic Dermatitis | Neuroblastoma | Carcinoma, Transitional Cell | Torticollis | Hypogonadism | VACTERL Association | Pregnancy, Ectopic | Erythematotelangiectatic Rosacea | Autoimmune Hemolytic Anemia | Hypothyroidism | Hereditary Multiple Exostoses | Epidermolysis Bullosa Simplex, Localized | Urticaria | Sarcoma, Alveolar Soft Part | CHOPS Syndrome | Stuttering | Pure Autonomic Failure | Prolymphocytic Leukemia | Lymphoma, Primary Cutaneous Anaplastic Large Cell | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Melanoma, Uveal | Gastritis | Essential Fructosuria | Scapuloperoneal Spinal Muscular Atrophy | LRBA Deficiency | Camptocormia | Cyst | Hemophagocytic Lymphohistiocytosis | Peters-plus Syndrome | Neuroma | Disseminated Intravascular Coagulation | Hyperinsulinism-hyperammonemia Syndrome | Intermittent Explosive Disorder | Juvenile Polyposis | Danon Disease | Pathological Gambling | Hemorrhage | Pfeiffer Syndrome | Blepharospasm | Crisponi Syndrome | Bernard-Soulier Syndrome | Long QT Syndrome Type 3 | Pierson Syndrome | Alopecia Totalis | Pyloric Stenosis, Infantile Hypertrophic | Hepatitis D | Moyamoya Disease | Farber Disease | Kohlschutter-Tonz Syndrome | Aspartylglycosaminuria | Reflex Epilepsy | Kleine-Levin Syndrome | Meleda Disease | Epilepsy | Cancer, Skin | H Syndrome | Marshall-Smith Syndrome | Tinea Versicolor | Majeed Syndrome | Diffuse Intrinsic Pontine Glioma | Keratoacanthoma | Tuberculous Meningitis | Olmsted Syndrome | Autonomic Neuropathy | Sporadic Hemiplegic Migraine | Premature Ejaculation | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Anovulation | Down Syndrome | Asperger Syndrome | Charcot-Marie-Tooth Disease Type 2T | Batten Disease | Retinal Degeneration | Papillon-Lefevre Syndrome | Fibromuscular Dysplasia | Vertebrobasilar Insufficiency | Congenital Diaphragmatic Hernia | Pleurisy | Wolman Disease | Lipid Metabolism Disorders | Axenfeld-Rieger Syndrome | Stiff-man Syndrome | Pancytopenia | 3-methylglutaconic Aciduria | Acute Kidney Injury | Parapsoriasis | Cryptococcal Meningitis | Congenital Hereditary Endothelial Dystrophy Type I | Epithelioid Hemangioma | Graft-versus-host Disease | Pendred Syndrome | Rash | Leishmaniasis, Cutaneous | Ichthyosis Bullosa Of Siemens | Familial Exudative Vitreoretinopathy | VACTERL/VATER Association | Christianson Syndrome | X-linked Sideroblastic Anemia | Hypoplastic Left Heart Syndrome | Tyrosinemia Type 1 | Cholelithiasis | Keratosis, Seborrheic | Neurodevelopmental Disorders | Superficial Spreading Melanoma | Phenylketonuria | Crimean-Congo Hemorrhagic Fever | Hepatitis E | Johanson-Blizzard Syndrome | Osteomyelitis | Carney Triad | Sturge-Weber Syndrome | Primrose Syndrome | Pycnodysostosis | Adrenoleukodystrophy, X-linked | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Charcot-Marie-Tooth Disease, Type 2C | Long QT Syndrome Type 1 | Nephronophthisis | Benign Familial Neonatal Convulsions | Atrioventricular Septal Defect | Multicentric Carpotarsal Osteolysis Syndrome | Steel Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Hypohidrotic Ectodermal Dysplasia | Silver-Russell Syndrome | Harlequin Ichthyosis | 3-M Syndrome | Hypertension, Renovascular | Periventricular Nodular Heterotopia | Paraganglioma | Cartilage Disorders | Lentigo | Cheilitis | Hypolipoproteinemia | Fragile X Syndrome | Multiple Hamartoma Syndrome | Occipital Neuralgia | Pyelonephritis | Spinal And Bulbar Muscular Atrophy | Otosclerosis | Spinocerebellar Ataxia | Craniofrontonasal Syndrome | Glycogen Storage Disease Type 5 | Gout | Trimethylaminuria | Central Pain Syndrome | Tyrosinemia | Leiomyoma | Congestive Heart Failure | Acromesomelic Dysplasia | Familial Pheochromocytoma-paraganglioma | Achromatopsia | Keloid | Schuurs-Hoeijmakers Syndrome | Iron Deficiency Anemia | Anxiety Disorders | Blau Syndrome | Menkes Disease | Hidradenitis Suppurativa | Renal Dysplasia | Malaria | Persistent Mullerian Duct Syndrome | Sclerosteosis | Burn-McKeown Syndrome | Chronic Idiopathic Myelofibrosis | Carcinoma In Situ | Adenoid Cystic Carcinoma | Globozoospermia | Mountain Sickness | Early Infantile Epileptic Encephalopathy | Papilledema | Choroideremia | Nevus | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Paroxysmal Nocturnal Hemoglobinuria | Primary Hyperoxaluria Type 1 | Hyperkeratosis | Geleophysic Dysplasia | Sjogren Syndrome | Angina Pectoris | Pontocerebellar Hypoplasia | Gyrate Atrophy Of The Choroid And Retina | Common Cold | Neurofibromatosis-Noonan Syndrome | Pseudohermaphroditism | Cleidocranial Dysplasia | Desmosterolosis | Stuve-Wiedemann Syndrome | Mucolipidosis Type II | Hepatic Veno-occlusive Disease | Poretti-Boltshauser Syndrome | Acute Anterior Uveitis | Thanatophoric Dysplasia | Takenouchi-Kosaki Syndrome | Phenylketonuria II | Hyperuricemic Nephropathy, Familial Juvenile | Albinism | Stroke, Ischemic | Chordoma | Astigmatism | Nephrotic Syndrome | Palmoplantar Keratoderma | Cockayne Syndrome | Fibronectin Glomerulopathy | Glaucomatocyclitic Crisis | Peeling Skin Syndrome, Acral Type | Coenzyme Q10 Deficiency | Tracheal Disorders | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Peyronie's Disease | Hemorrhoids | Spinocerebellar Ataxia Type 6 | Cold Agglutinin Disease | Alveolar Capillary Dysplasia | Wiedemann-Steiner Syndrome | Periodic Limb Movement Disorder | Succinic Semialdehyde Dehydrogenase Deficiency | Hypertension, Pulmonary | Progressive Familial Intrahepatic Cholestasis Type 1 | Iron Metabolism Disorders | Autosomal Recessive Spastic Paraplegia Type 54 | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Shprintzen-Goldberg Syndrome | Herpes Simplex Dermatitis | Parkinson's Disease | Charcot-Marie-Tooth Disease Type 3 | Osteogenesis Imperfecta Type III | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Cancer, Breast | Prune Belly Syndrome | Waardenburg Syndrome Type 4 | Cholangitis | Bone Marrow Necrosis | Infantile Nephropathic Cystinosis | Congenital Disorders Of Glycosylation | Skin Fragility-woolly Hair Syndrome | Macular Corneal Dystrophy | Spinocerebellar Ataxia Type 20 | Meningococcal Infections | Palsy, Cerebral | Congenital Generalized Lipodystrophy | Stroke | Schwartz-Jampel-Aberfeld Syndrome | Acrodermatitis Enteropathica | Synpolydactyly | Ileitis | Temtamy Preaxial Brachydactyly Syndrome | Leprosy | Chitayat Syndrome | Tylosis With Esophageal Cancer | Agoraphobia | Hypersomnia | Thrombasthenia | Micro Syndrome | Paraplegia | Holt-Oram Syndrome | Mandibuloacral Dysplasia With Type A Lipodystrophy | Renal Tubular Acidosis | Vici Syndrome | Heterotopic Ossification | Macrophage Activation Syndrome | Alpha-thalassemia Myelodysplasia Syndrome | Cardiomyopathy, Peripartum | Seminoma | NGLY1 Deficiency | Krabbe Disease | Multiple Sclerosis, Chronic Progressive | Inflammatory Bowel Disease | Wilson's Disease | Acute Generalized Exanthematous Pustulosis | Leukoplakia, Oral | Varices | Spondylocostal Dysostosis | Zellweger Syndrome | Myofibrillar Myopathy | Monilethrix | Diffuse Palmoplantar Keratoderma | Encephalopathy, Ethylmalonic | Arthritis, Psoriatic | Homocystinuria | Pernicious Anemia | Paronychia | Chanarin-Dorfman Syndrome | Perivascular Epithelioid Cell Tumor | Myotonia | Common Variable Immunodeficiency | Amelogenesis Imperfecta | Fuchs Dystrophy | Blue Rubber Bleb Nevus Syndrome | Autosomal Recessive Bestrophinopathy | Granuloma Annulare | Chiari Malformation Type I | Peritonitis | Greenberg Dysplasia | Optic Nerve Hypoplasia, Bilateral | Diabetic Neuropathy | Avellino Corneal Dystrophy | Colon Adenoma | Hyperacusis | L-2-Hydroxyglutaric Aciduria | Headache | Portal Vein Thrombosis | Hyperuricemia | Gilbert Syndrome | Ornithine Transcarbamylase Deficiency | Antiphospholipid Syndrome | Renal Failure | Diastrophic Dysplasia | DICER1 Syndrome | Arthritis | Spondyloperipheral Dysplasia | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Vitamin K Deficiency | Spinocerebellar Ataxia Type 27 | McKusick Type Metaphyseal Chondrodysplasia | Hypospadias | Non-bullous Congenital Ichthyosiform Erythroderma | Dystonia | Huntington's Disease | Temporal Lobe Epilepsy | Non-Hodgkin Lymphoma | Impulse Control Disorder | Chronic Myelomonocytic Leukemia | Megaloblastic Anemia | Blepharoconjunctivitis | Rhinitis | Ligneous Conjunctivitis | Corneal Edema | Amish Infantile Epilepsy Syndrome | Lesch-Nyhan Syndrome | Rhizomelic Chondrodysplasia Punctata | Ovarian Hyperstimulation Syndrome
