| Disease Browser
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Parent Node:
 Blood Coagulation Disorders (D001778) |
Parent Node:
Genetic Diseases, Inborn (D030342) |
..Starting node
.. Blood Coagulation Disorders, Inherited (D025861)
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Child Nodes:
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........Activated Protein C Resistance (D020016)  1 |
| ........Afibrinogenemia (D000347) 3 |
| ........Antithrombin III Deficiency (D020152) |
| ........Athrombia, Essential (C565927) |
| ........Bernard-Soulier Syndrome (D001606) 5 |
| ........Bleeding Disorder Due To P2RY12 Defect (C565220) |
| ........Dysprothrombinemia (C562724) |
| ........Factor V Deficiency (D005166) 4 |
| ........Factor VII Deficiency (D005168) |
| ........Factor X Deficiency (D005171) |
| ........Factor XI Deficiency (D005173) |
| ........Factor XII Deficiency (D005175) |
| ........Factor XIII Deficiency (D005177) 2 |
| ........Factors VIII, IX And XI, Combined Deficiency of (C565023) |
| ........Familial Multiple Coagulation Factor Deficiency II (C565024) |
| ........Familial Multiple Coagulation Factor Deficiency IV (C565025) |
| ........Familial Multiple Coagulation Factor Deficiency VI (C565022) |
| ........Gray Platelet Syndrome (D055652) 1 |
| ........Hemophilia A (D006467) 5 |
| ........Hemophilia B (D002836) |
| ........Hermanski-Pudlak Syndrome (D022861) 3 |
| ........Hypoprothrombinemias (D007020) 2 |
| ........Passovoy Factor (C566820) |
| ........Pechet Factor Deficiency (C566814) |
| ........Platelet Disorder, Familial, with Associated Myeloid Malignancy (C563324) |
| ........Prolonged Bleeding Time, Brachydactyly, and Mental Retardation (C564207) |
| ........Protein C Deficiency (D020151) 5 |
| ........Thrombasthenia (D013915) 3 |
| ........Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1 (C564741) |
| ........Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, Type 2 (C564393) |
| ........von Willebrand Diseases (D014842) 6 |
| ........Wiskott-Aldrich Syndrome (D014923) 1 |
Sister Nodes: |
..ACTH Deficiency, Isolated (C562707)
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..Adrenal Hyperplasia, Congenital (D000312) 12
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..Adrenocortical Hypofunction, Chronic Primary Congenital (C562711)
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..Alagille Syndrome (D016738)
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..alpha 1-Antitrypsin Deficiency (D019896) 1
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..Alpha-2-Deficient Collagen Disease (C565963)
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..Anemia, Hemolytic, Congenital (D000745) 68
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..Anemia, Hypoplastic, Congenital (D029502) 27
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..Angioedemas, Hereditary (D054179) 2
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..Ataxia Telangiectasia (D001260) 6
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..Atrial Standstill (C563984)
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..Autoimmune Lymphoproliferative Syndrome (D056735) 5
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..Blood Coagulation Disorders, Inherited (D025861) 70
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..Brugada Syndrome (D053840) 9
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..CADASIL (D046589) 1
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..Camurati-Engelmann Syndrome (D003966) 4
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..Cardiomyopathy, Hypertrophic, Familial (D024741) 15
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..Cerebral Palsy, Ataxic, Autosomal Recessive (C562856)
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..CHARGE Syndrome (D058747)
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..Cherubism (D002636) 2
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..Chromosome Disorders (D025063) 160
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..Cirrhosis, Familial (C566123)
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..Complement Factor I Deficiency (C572568)
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..Corticosteroid-Binding Globulin Deficiency (C565152)
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..Costello Syndrome (D056685)
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..Cryoglobulinemia, Familial Mixed (C565141)
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..Cystic Fibrosis (D003550) 4
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..Donohue Syndrome (D056731) 1
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..Dwarfism (D004392) 155
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..Epistaxis, Hereditary (C562751)
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..Eye Diseases, Hereditary (D015785) 373
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..Frasier Syndrome (D052159)
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..Genetic Diseases, X-Linked (D040181) 412
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..Genetic Diseases, Y-Linked (D050174) 5
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..Hajdu-Cheney Syndrome (D031845) 1
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..Hemoglobinopathies (D006453) 23
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..Hepatic Fibrosis, Congenital (C562378)
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..Hereditary Autoinflammatory Diseases (D056660) 10
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..Hereditary Myopathy with Early Respiratory Failure (C566343)
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..Heredodegenerative Disorders, Nervous System (D020271) 543
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..Histiocytosis, Familial Lipochrome (C562738)
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..Hyper-IgM Immunodeficiency Syndrome (D053306) 3
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..Hyperthyroxinemia, Familial Dysalbuminemic (D050010) 1
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..Interstitial Pneumonitis, Desquamative, Familial (C562470)
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..Kallmann Syndrome (D017436) 9
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..Kartagener Syndrome (D007619) 6
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..Lennox Gastaut Syndrome (D065768) 1
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..Loeys-Dietz Syndrome (D055947) 5
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..Marfan Syndrome (D008382) 9
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..Metabolism, Inborn Errors (D008661) 886
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..Muscular Dystrophies (D009136) 117
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..Myasthenic Syndromes, Congenital (D020294) 15
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..Nail-Patella Syndrome (D009261) 1
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..Neoplastic Syndromes, Hereditary (D009386) 111
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..Neutropenia, Nonimmune Chronic Idiopathic, Adult (C564320)
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..Osteoarthropathy, Primary Hypertrophic (D010004) 2
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..Osteogenesis Imperfecta (D010013) 27
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..Pain Insensitivity, Congenital (D000699) 2
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..Parotidomegaly, Hereditary Bilateral (C566821)
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..Pelger-Huet Anomaly (D010381)
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..Platelet Glycoprotein IV Deficiency (C564245)
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..Polycystic Kidney, Autosomal Recessive (D017044) 3
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..Prolactin Deficiency, Isolated (C562708)
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..Pulmonary Alveolar Microlithiasis (C562405)
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..Pycnodysostosis (D058631)
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..Rh Deficiency Syndrome (C562717)
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..Skin Diseases, Genetic (D012873) 462
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..Weill-Marchesani Syndrome (D056846)
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..Werner Syndrome (D014898) 1
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..Yellow Nail Syndrome (D056684) 1
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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