DISEASES Hemic and Lymphatic Diseases [C15] Hemic and Lymphatic Diseases Hematologic Diseases [C15.378] Hematologic Diseases Blood Coagulation Disorders [C15.378.100] Blood Coagulation Disorders Blood Coagulation Disorders, Inherited [C15.378.100.100] Blood Coagulation Disorders, Inherited Activated Protein C Resistance [C15.378.100.100.037] Activated Protein C Resistance Afibrinogenemia [C15.378.100.100.056] Afibrinogenemia Antithrombin III Deficiency [C15.378.100.100.075] Antithrombin III Deficiency Bernard-Soulier Syndrome [C15.378.100.100.080] Bernard-Soulier Syndrome Factor V Deficiency [C15.378.100.100.300] Factor V Deficiency Factor VII Deficiency [C15.378.100.100.310] Factor VII Deficiency Factor X Deficiency [C15.378.100.100.320] Factor X Deficiency Factor XI Deficiency [C15.378.100.100.325] Factor XI Deficiency Factor XII Deficiency [C15.378.100.100.330] Factor XII Deficiency Factor XIII Deficiency [C15.378.100.100.335] Factor XIII Deficiency Hemophilia A [C15.378.100.100.500] Hemophilia A Hemophilia B [C15.378.100.100.510] Hemophilia B Hermanski-Pudlak Syndrome [C15.378.100.100.515] Hermanski-Pudlak Syndrome Hypoprothrombinemias [C15.378.100.100.550] Hypoprothrombinemias Protein C Deficiency [C15.378.100.100.690] Protein C Deficiency Thrombasthenia [C15.378.100.100.820] Thrombasthenia von Willebrand Diseases [C15.378.100.100.900] von Willebrand Diseases Wiskott-Aldrich Syndrome [C15.378.100.100.970] Wiskott-Aldrich Syndrome Coagulation Protein Disorders [C15.378.100.141] Coagulation Protein Disorders Disseminated Intravascular Coagulation [C15.378.100.220] Disseminated Intravascular Coagulation Ecchymosis [C15.378.100.452] Ecchymosis Platelet Storage Pool Deficiency [C15.378.100.685] Platelet Storage Pool Deficiency Protein S Deficiency [C15.378.100.800] Protein S Deficiency Purpura [C15.378.100.802] Purpura Thrombocythemia, Essential [C15.378.100.832] Thrombocythemia, Essential Thromboinflammation [C15.378.100.876] Thromboinflammation Vitamin K Deficiency [C15.378.100.920] Vitamin K Deficiency DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Genetic Diseases, Inborn [C16.320] Genetic Diseases, Inborn Adrenal Hyperplasia, Congenital [C16.320.033] Adrenal Hyperplasia, Congenital Alagille Syndrome [C16.320.051] Alagille Syndrome alpha 1-Antitrypsin Deficiency [C16.320.060] alpha 1-Antitrypsin Deficiency Anemia, Hemolytic, Congenital [C16.320.070] Anemia, Hemolytic, Congenital Anemia, Hypoplastic, Congenital [C16.320.077] Anemia, Hypoplastic, Congenital Ataxia Telangiectasia [C16.320.080] Ataxia Telangiectasia Autoimmune Lymphoproliferative Syndrome [C16.320.089] Autoimmune Lymphoproliferative Syndrome Blood Coagulation Disorders, Inherited [C16.320.099] Blood Coagulation Disorders, Inherited Activated Protein C Resistance [C16.320.099.037] Activated Protein C Resistance Afibrinogenemia [C16.320.099.056] Afibrinogenemia Antithrombin III Deficiency [C16.320.099.075] Antithrombin III Deficiency Bernard-Soulier Syndrome [C16.320.099.080] Bernard-Soulier Syndrome Factor V Deficiency [C16.320.099.300] Factor V Deficiency Factor VII Deficiency [C16.320.099.310] Factor VII Deficiency Factor X Deficiency [C16.320.099.320] Factor X Deficiency Factor XI Deficiency [C16.320.099.325] Factor XI Deficiency Factor XII Deficiency [C16.320.099.330] Factor XII Deficiency Factor XIII Deficiency [C16.320.099.335] Factor XIII Deficiency Gray Platelet Syndrome [C16.320.099.417] Gray Platelet Syndrome Hemophilia A [C16.320.099.500] Hemophilia A Hemophilia B [C16.320.099.510] Hemophilia B Hermanski-Pudlak Syndrome [C16.320.099.515] Hermanski-Pudlak Syndrome Hypoprothrombinemias [C16.320.099.550] Hypoprothrombinemias Protein C Deficiency [C16.320.099.690] Protein C Deficiency Thrombasthenia [C16.320.099.820] Thrombasthenia von Willebrand Diseases [C16.320.099.920] von Willebrand Diseases Wiskott-Aldrich Syndrome [C16.320.099.970] Wiskott-Aldrich Syndrome Brugada Syndrome [C16.320.100] Brugada Syndrome CADASIL [C16.320.129] CADASIL Camurati-Engelmann Syndrome [C16.320.144] Camurati-Engelmann Syndrome Cardiomyopathy, Hypertrophic, Familial [C16.320.160] Cardiomyopathy, Hypertrophic, Familial CHARGE Syndrome [C16.320.165] CHARGE Syndrome Cherubism [C16.320.170] Cherubism Chromosome Disorders [C16.320.180] Chromosome Disorders Ciliopathies [C16.320.184] Ciliopathies Costello Syndrome [C16.320.188] Costello Syndrome Cystic Fibrosis [C16.320.190] Cystic Fibrosis Donohue Syndrome [C16.320.215] Donohue Syndrome Dwarfism [C16.320.240] Dwarfism Eye Diseases, Hereditary [C16.320.290] Eye Diseases, Hereditary Familial Multiple Lipomatosis [C16.320.298] Familial Multiple Lipomatosis Frasier Syndrome [C16.320.306] Frasier Syndrome GATA2 Deficiency [C16.320.314] GATA2 Deficiency Genetic Diseases, X-Linked [C16.320.322] Genetic Diseases, X-Linked Genetic Diseases, Y-Linked [C16.320.338] Genetic Diseases, Y-Linked Hajdu-Cheney Syndrome [C16.320.355] Hajdu-Cheney Syndrome Hemoglobinopathies [C16.320.365] Hemoglobinopathies Hereditary Autoinflammatory Diseases [C16.320.382] Hereditary Autoinflammatory Diseases Heredodegenerative Disorders, Nervous System [C16.320.400] Heredodegenerative Disorders, Nervous System Hyper-IgM Immunodeficiency Syndrome [C16.320.413] Hyper-IgM Immunodeficiency Syndrome Hyperthyroxinemia, Familial Dysalbuminemic [C16.320.427] Hyperthyroxinemia, Familial Dysalbuminemic Imprinting Disorders [C16.320.447] Imprinting Disorders Kallmann Syndrome [C16.320.467] Kallmann Syndrome Kartagener Syndrome [C16.320.480] Kartagener Syndrome Laminopathies [C16.320.488] Laminopathies Lennox Gastaut Syndrome [C16.320.495] Lennox Gastaut Syndrome Loeys-Dietz Syndrome [C16.320.510] Loeys-Dietz Syndrome Marfan Syndrome [C16.320.540] Marfan Syndrome Metabolism, Inborn Errors [C16.320.565] Metabolism, Inborn Errors Muscular Dystrophies [C16.320.577] Muscular Dystrophies Myasthenic Syndromes, Congenital [C16.320.590] Myasthenic Syndromes, Congenital Nail-Patella Syndrome [C16.320.600] Nail-Patella Syndrome Neoplastic Syndromes, Hereditary [C16.320.700] Neoplastic Syndromes, Hereditary Oculocerebrorenal Syndrome [C16.320.709] Oculocerebrorenal Syndrome Orofaciodigital Syndromes [C16.320.714] Orofaciodigital Syndromes Osteoarthropathy, Primary Hypertrophic [C16.320.718] Osteoarthropathy, Primary Hypertrophic Osteochondrodysplasias [C16.320.728] Osteochondrodysplasias Osteogenesis Imperfecta [C16.320.737] Osteogenesis Imperfecta Pain Insensitivity, Congenital [C16.320.775] Pain Insensitivity, Congenital Pelger-Huet Anomaly [C16.320.784] Pelger-Huet Anomaly Primary Immunodeficiency Diseases [C16.320.798] Primary Immunodeficiency Diseases Pycnodysostosis [C16.320.812] Pycnodysostosis Renal Tubular Transport, Inborn Errors [C16.320.831] Renal Tubular Transport, Inborn Errors Skin Diseases, Genetic [C16.320.850] Skin Diseases, Genetic Werner Syndrome [C16.320.925] Werner Syndrome Yellow Nail Syndrome [C16.320.962] Yellow Nail Syndrome

Blood Coagulation Disorders, Inherited - Preferred

Concept UI	M0376236
Scope note	Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.
Preferred term	Blood Coagulation Disorders, Inherited
Entry term(s)	Coagulation Disorder, Hereditary Coagulation Disorder, Inherited Coagulation Disorders, Hereditary Coagulation Disorders, Inherited Hereditary Blood Coagulation Disorders Hereditary Coagulation Disorder Hereditary Coagulation Disorders Inherited Blood Coagulation Disorders Inherited Coagulation Disorder Inherited Coagulation Disorders