Related MeSH Hierarchy (4)
Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Blood Coagulation Disorders » Blood Coagulation Disorders, Inherited » Hemophilia A
Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Blood Coagulation Disorders » Coagulation Protein Disorders » Hemophilia A
Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Hemorrhagic Disorders » Hemophilia A
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Blood Coagulation Disorders, Inherited » Hemophilia A
Description
The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage. MeSH
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Approved Indicated Drugs (16)
antihemophilic factor (recombinant), fc-vwf-xten fusion protein-ehtl (ALTUVIIIO)
antihemophilic factor viii human (Hemofil M)
antihemophilic factor viii (Recombinant) (Adynovate)
antihemophilic factor viii (Recombinant), Fc-fusion protein (Eloctate)
Phase 4 Indicated Drugs (16)
Phase 3 Indicated Drugs (16)
Phase 2 Indicated Drugs (8)
Phase 1 Indicated Drugs (14)
Organization Involved with Phase 4 Indications (51)
Bankura Sammilani Medical College
Baqiyatallah Medical Sciences University
Indiana Hemophilia & Thrombosis Center
Iranian Blood Transfusion Research Center
Mountain States Regional Hemophilia Center, Aurora, Columbia
Organization Involved with Phase 3 Indications (54)
Health Resources and Services Administration (HRSA)
Icahn School of Medicine at Mount Sinai
Jiangsu Chia-tai Tianqing Pharmaceutical Co.,Ltd
Laboratoire français de Fractionnement et de Biotechnologies
Memorial Hermann Health System
Organization Involved with Phase 2 Indications (35)
Organization Involved with Phase 1 Indications (19)
Organization Involved with Other Experimental Indications (13)
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UMLS Data
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