Disease

Vitamin K Deficiency

About the Disease
Vitamin K Deficiency Bleeding, also known as vitamin k deficiency, is related to vitamin k-dependent clotting factors, combined deficiency of, 2 and vitamin k-dependent clotting factors, combined deficiency of, 1. An important gene associated with Vitamin K Deficiency Bleeding is F2 (Coagulation Factor II, Thrombin), and among its related pathways/superpathways are Metabolism of proteins and Response to elevated platelet cytosolic Ca2+. The drugs Dabigatran and Edoxaban have been mentioned in the context of this disorder. Affiliated tissues include kidney, liver and bone, and related phenotypes are no effect and no effect

Common Targets
GGCX

疾病靶点研报
Vitamin K Deficiency

Note: If you'd like to get a target analysis report for Vitamin K Deficiency, 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 Vitamin K Deficiency at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Hemimegalencephaly | Basal Cell Nevus Syndrome | Nicotine Addiction | Pain | Pseudohermaphroditism | Mast Cell Leukemia | Omenn Syndrome | Mabry Syndrome | Spinal Muscular Atrophy Type 2 | Pemphigoid | Hypophosphatasia | Acute Kidney Injury | Crigler-Najjar Syndrome | Pituitary Dwarfism | Niemann-Pick Disease | Uremic Pruritus | Urofacial Syndrome | Sarcomatoid Carcinoma Of The Lung | Sjogren Syndrome | Lipid Storage Myopathy | Meningioma, Benign | Creatine Deficiency Syndrome | Weill-Marchesani Syndrome | Megaloblastic Anemia | Adenoid Cystic Carcinoma | Spinal Cord Diseases | Achromatopsia | Angelman Syndrome | Sarcoma, Alveolar Soft Part | Primary Familial Brain Calcification | Encephalitis, Tick-borne | Pupil Disorders | Blue Nevus | Majeed Syndrome | Aneurysm, Abdominal Aortic | Hyperkeratosis | Benign Familial Pemphigus | Kearns-Sayre Syndrome | McCune-Albright Syndrome | Goiter | Charcot-Marie-Tooth Disease Type 4 | Fraser Syndrome | Skin Fragility-woolly Hair Syndrome | Adenosine Deaminase 2 Deficiency | Growth Hormone Excess | Fundus Albipunctatus | Inborn Errors Of Metabolism | Nijmegen Breakage Syndrome | Long QT Syndrome Type 2 | Cramp Fasciculation Syndrome | Hepatoblastoma | Scabies | Sick Sinus Syndrome | Papillon-Lefevre Syndrome | Rheumatic Heart Disease | Poirier-Bienvenu Neurodevelopmental Syndrome | Clouston Hidrotic Ectodermal Dysplasia | Renal Hypomagnesemia 3 | Spitzoid Melanoma | Blue Rubber Bleb Nevus Syndrome | Mitochondrial DNA Depletion Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Giant Axonal Neuropathy | Marfan Syndrome | Aldosteronism | Gynecomastia | Hypotonia-cystinuria Syndrome | Oculopharyngeal Muscular Dystrophy | Auriculocondylar Syndrome | Charcot-Marie-Tooth Disease, Type 2 | Pierpont Syndrome | KBG Syndrome | Epilepsy | Scapuloperoneal Myopathy, X-linked Dominant | Barakat Syndrome | Combined Pituitary Hormone Deficiency | Blastomycosis | Multiple Epiphyseal Dysplasia | Cryptococcal Meningitis | Congenital Disorders Of Glycosylation | Personality Disorders | Methylmalonic Aciduria And Homocystinuria, CblC Type | Adenomatoid Tumor | McLeod Syndrome | Hypertension, Portal | Cancer, Skin | Ischemia | Veno-occlusive Disease | Spinocerebellar Ataxia | Coffin-Lowry Syndrome | Erdheim-Chester Disease | Persistent Hyperplastic Primary Vitreous | Lichen Planus | Malaria | Sarcoidosis | Cluster Headache | Avellino Corneal Dystrophy | Mitochondrial Myopathy | Tuberculous Meningitis | Bare Lymphocyte Syndrome | Esophagitis | Muscular Dystrophy | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | GM2-gangliosidosis AB Variant | Lamellar Ichthyosis | Rothmund-Thomson Syndrome | Castleman Disease | Polycythemia | Noonan Syndrome-like Disorder With Loose Anagen Hair | Lateral Meningocele Syndrome | Essential Fructosuria | Osteoporosis-pseudoglioma Syndrome | Kernicterus | Arts Syndrome | Postpartum Depression | Antithrombin III Deficiency | Epidermolytic Hyperkeratosis | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Vitamin K Deficiency | Posterior Polar Cataract | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Anorexia Nervosa | Holt-Oram Syndrome | Lipodystrophy | Basal Ganglia Cerebrovascular Disease | Myocardial Infarction | Erythrokeratodermia Variabilis | Angioedema, Hereditary | Meesmann Corneal Dystrophy | Alstrom Syndrome | Primary Carnitine Deficiency | Spinocerebellar Ataxia Type 20 | Nager Acrofacial Dysostosis | PHARC Syndrome | Polycystic Ovary Syndrome | Larsen Syndrome | Postaxial Polydactyly | Hypervalinemia | Hereditary Pyropoikilocytosis | Albinism | Distal Myopathy 2 | Cardiac Sarcoidosis | Congenital Nystagmus | Pseudohypoparathyroidism Type 1A | Congenital Dyserythropoietic Anemia Type 4 | Chronic Periodontitis | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | McKusick Type Metaphyseal Chondrodysplasia | Polymyositis | Brachial Plexus Neuropathy | Polydactyly | Familial Dysautonomia | Familial Mediterranean Fever | Congenital Aniridia | Retinal Diseases | Nephrocalcinosis | Benign Recurrent Intrahepatic Cholestasis 1 | Presbyopia | Pyelonephritis | Cardiomyopathy, Dilated, 1L | Pemphigus Foliaceus | Split Hand-foot Malformation | Strabismus | Retinoschisis | Currarino Syndrome | Cone Dystrophy | Lymphedema | Infertility, Male | Johanson-Blizzard Syndrome | Acute Chest Syndrome | Gerodermia Osteodysplastica | Kleine-Levin Syndrome | Astigmatism | Cholangitis | Vitamin B12 Deficiency | Neurofibromatosis Type 2 | Asperger Syndrome | Dermatitis | Agnathia-Otocephaly Complex | Von Willebrand Disease | Inflammatory Joint Disease | Myositis, Focal | Progressive Familial Intrahepatic Cholestasis | Juvenile Myelomonocytic Leukemia | Analgesia | Spondylocarpotarsal Synostosis Syndrome | Arterial Tortuosity Syndrome | Metabolic Syndrome | Myofibromatosis | Cirrhosis | Raynaud Phenomenon | Autosomal Recessive Bestrophinopathy | Idiopathic Pulmonary Fibrosis | Danon Disease | Liver Failure, Acute Infantile | Burn-McKeown Syndrome | Williams Syndrome | Spastic Paraplegia Type 7 | Colon Adenoma | Fetal Alcohol Syndrome | Sotos Syndrome | Hypogonadism | Congenital Generalized Lipodystrophy | Cold-induced Sweating Syndrome | Allan-Herndon-Dudley Syndrome | Glycogen Storage Disease | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Diffuse Intrinsic Pontine Glioma | Thrombophlebitis | Hereditary Sensory Neuropathy Type 1 | Obsessive-compulsive Disorder | Sulfite Oxidase Deficiency | Mucolipidosis | Pheochromocytoma | Mycosis Fungoides | Myosin Storage Myopathy | Androgen Insensitivity | Neurofibroma, Plexiform | Multicentric Carpotarsal Osteolysis Syndrome | Crisponi Syndrome | Macular Corneal Dystrophy Type 1 | Autoimmune Polyendocrinopathy Syndrome Type I | Schistosomiasis | Spinocerebellar Ataxia Type 27 | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Pulmonary Veno-occlusive Disease | Hyperuricemia | Yellow Fever | Persistent Truncus Arteriosus | Non-Hodgkin Lymphoma | Primary Progressive Aphasia | Androgenic Alopecia | Cushing Syndrome | Lymphoproliferative Disorders | Agammaglobulinemia | Thrombophilia | Cryptosporidiosis | Carcinoma, Squamous Cell | Syncope | Aspartylglycosaminuria | Arthropathy | Chorea-acanthocytosis | Enterocolitis, Necrotizing | Phosphoglycerate Dehydrogenase Deficiency | Chronic Myelomonocytic Leukemia | Pericarditis | Pulmonary Alveolar Proteinosis | Progressive Encephalopathy-optic Atrophy Syndrome | Tendinopathy | Moyamoya Disease | Small Lymphocytic Lymphoma | Low Tension Glaucoma | Pneumonia, Bacterial | Cat Eye Syndrome | Keratosis, Actinic | Dominant Optic Atrophy | Otitis Media | Teratozoospermia | Keratitis-ichthyosis-deafness Syndrome | Short-chain Acyl-CoA Dehydrogenase Deficiency | Isovaleric Acidemia | T-cell Lymphoma, Subcutaneous Panniculitis-like | Congenital Torticollis | Dengue Shock Syndrome | Hemochromatosis | Chronic Beryllium Disease | Seborrheic Dermatitis | Lentigo | Asphyxia Neonatorum | Porphyria | Sick Sinus Syndrome 1 | Alpha-thalassemia Myelodysplasia Syndrome | Myoclonic Atonic Epilepsy | Neurofibroma | Chromosome 5q Deletion Syndrome | Huntington's Disease | Sleep Apnea, Central | Esotropia | Demyelinating Diseases | Erythema Nodosum | Lafora Disease | Osteogenesis Imperfecta Type I | Acrodermatitis | Bipolar Disorder | Amebiasis | Chondrodysplasia Punctata | Glycogen Storage Disease Type 1b | T-cell Leukemia | Ectopia Lentis, Isolated, Autosomal Recessive | Congenital Disorders Of Glycosylation Type II | Binge Eating Disorder | Glutaric Aciduria Type 3 | Myelitis, Transverse | Chondrodysplasia Punctata 1, X-linked Recessive | Pulmonary Tuberculosis | DiGeorge Syndrome | Purpura, Thrombotic Thrombocytopenic | Pure Autonomic Failure | Varices | Prolidase Deficiency | Systemic Mastocytosis | Spinocerebellar Ataxia Type 1 | Motor Neuron Diseases | Chronic Inflammatory Demyelinating Polyneuropathy | Cholecystitis | Hemorrhagic Disorders | Cholera | Anal Fissure | Paraganglioma, Carotid Body | Peeling Skin Syndrome, Acral Type | Nephrosclerosis | Porphyria, Acute Intermittent | Schamberg Disease | Major Depression | Niemann-Pick Disease, Type B | Trigonocephaly | Obesity, Morbid | Meningitis | Hemolytic Anemia | Epidermolytic Palmoplantar Keratoderma | Corneal Dystrophies, Hereditary | Leukoplakia | Riboflavin Transporter Deficiency Neuronopathy | Colitis, Collagenous | Multiple Sclerosis, Relapsing-remitting | Pleomorphic Xanthoastrocytoma | Carey-Fineman-Ziter Syndrome | Communication Disorders | Papilloma | Shprintzen-Goldberg Syndrome | Cranial Nerve Disease | Arthritis, Reactive | Diabetic Neuropathy | Acute Anterior Uveitis | Spinocerebellar Ataxia Type 5 | Asplenia | Infectious Diarrhea | T-cell Chronic Lymphocytic Leukemia | Frank-ter Haar Syndrome | Chronic Myeloid Leukemia | Leri Pleonosteosis | Lyme Disease | Gangliosidosis, GM1 | Hepatic Veno-occlusive Disease | Angiosarcoma Of The Breast | Blastoma, Pleuropulmonary | Vitiligo | Spinocerebellar Ataxia Type 21 | Rosacea | Spondylolisthesis | Vertebrobasilar Insufficiency | Congenital Adrenal Hyperplasia 1 | Waardenburg Syndrome Type 2A | Postpoliomyelitis Syndrome | Hypopituitarism | Traboulsi Syndrome | Primary Hyperoxaluria | Lymphangiomatosis | Hypertension, Essential | Fuchs Heterochromic Iridocyclitis | Hyperinsulinism-hyperammonemia Syndrome | Pterygium | Retinal Vasculitis | Granular Corneal Dystrophy | Heterotopic Ossification | Glycogen Storage Disease Type 4 | Restrictive Dermopathy | Anorectal Fistula | Erectile Dysfunction | Thymoma, Malignant | 3-methylglutaconic Aciduria Type IV | Osteogenesis Imperfecta Type II | Angiosarcoma | Congenital Central Hypoventilation Syndrome | Exocrine Pancreatic Insufficiency | Episodic Ataxia Type 1 | Sclerosteosis 2 | Cystitis | Spinocerebellar Ataxia Type 8 | Necrobiosis Lipoidica | Withdrawal Syndrome | Glioblastoma | Vitamin A Deficiency | Transthyretin-related Amyloidosis | Bardet-Biedl Syndrome | Kaposiform Hemangioendothelioma | Empyema | Waardenburg Syndrome Type 4A | Nephritis, Interstitial | Central Core Disease | Cabezas Syndrome | Early Infantile Epileptic Encephalopathy | Turner's Syndrome | Neurodegeneration With Brain Iron Accumulation | Aldosterone Synthase Deficiency | Limb Girdle Muscular Dystrophy | Succinic Semialdehyde Dehydrogenase Deficiency | Bulimia Nervosa | Constipation | Gout