Clinical Trials Involving Rare Diseases: F
- FACES Syndrome (4)
- FMR1-related Primary Ovarian Insufficiency (3)
- FOXG1 Syndrome (1)
- Fabry Disease (193)
- Facioscapulohumeral Muscular Dystrophy (50)
- Factor V Deficiency (1)
- Factor VII Deficiency (6)
- Factor X Deficiency (4)
- Factor XI Deficiency (3)
- Factor XII Deficiency (1)
- Factor XIII Deficiency (12)
- Fallopian Tube Cancer (714)
- Familial Adenomatous Polyposis (75)
- Familial Alzheimer Disease (2,924)
- Familial Atrial Fibrillation (2)
- Familial Cerebral Cavernous Malformation (13)
- Familial Chylomicronemia Syndrome (14)
- Familial Cold Autoinflammatory Syndrome (20)
- Familial Colorectal Cancer (7)
- Familial Deafness (1)
- Familial Dermographism (3)
- Familial Dilated Cardiomyopathy (4)
- Familial Dysautonomia (12)
- Familial Encephalopathy With Neuroserpin Inclusion Bodies (2)
- Familial Exudative Vitreoretinopathy (2)
- Familial HDL Deficiency (2)
- Familial Hemiplegic Migraine (4)
- Familial Hemophagocytic Lymphohistiocytosis (10)
- Familial Hypertrophic Cardiomyopathy (5)
- Familial Hypobetalipoproteinemia (10)
- Familial Hypocalciuric Hypercalcemia (2)
- Familial Isolated Hyperparathyroidism (2)
- Familial Isolated Pituitary Adenoma (1)
- Familial Joint Instability Syndrome (1)
- Familial LCAT Deficiency (1)
- Familial Lipoprotein Lipase Deficiency (25)
- Familial Mediterranean Fever (158)
- Familial Multiple Lipomatosis (1)
- Familial Pancreatic Cancer (18)
- Familial Partial Lipodystrophy (10)
- Familial Partial Lipodystrophy Type 2 (6)
- Familial Porencephaly (1)
- Familial Prostate Cancer (6)
- Familial Thoracic Aortic Aneurysm and Aortic Dissection (3)
- Familial Thyroglossal Duct Cyst (1)
- Familial Transthyretin Amyloidosis (78)
- Familial Tumoral Calcinosis (1)
- Fanconi Anemia (96)
- Fanconi Syndrome (105)
- Farber Disease (2)
- Fascioliasis (2)
- Fatal Familial Insomnia (7)
- Fatty Acid Hydroxylase-associated Neurodegeneration (1)
- Felty's Syndrome (1)
- Fetal Macrosomia (22)
- Fetal Thalidomide Syndrome (8)
- Fetal and Neonatal Alloimmune Thrombocytopenia (4)
- Fibrillary Glomerulonephritis (1)
- Fibrinogen Deficiency, Congenital (9)
- Fibrodysplasia Ossificans Progressiva (19)
- Fibrolamellar Carcinoma (13)
- Fibrosarcoma (120)
- Fibrous Dysplasia (28)
- Florid Cemento-osseous Dysplasia (1)
- Focal Cortical Dysplasia of Taylor (2)
- Focal Dermal Hypoplasia (5)
- Focal Segmental Glomerulosclerosis (86)
- Focal Task-specific Dystonia (54)
- Follicular Lymphoma (1,302)
- Fournier Gangrene (12)
- Fowler's Syndrome (3)
- Fragile X Syndrome (89)
- Fraser Syndrome (1)
- Frasier Syndrome (2)
- Freeman-Sheldon Syndrome (4)
- Frey's Syndrome (3)
- Friedreich Ataxia (80)
- Frontal Fibrosing Alopecia (9)
- Frontotemporal Dementia (246)
- Frontotemporal Dementia, Ubiquitin-positive (246)
- Fryns Syndrome (1)
- Fucosidosis (9)
- Fumarase Deficiency (2)
- Functioning Pancreatic Endocrine Tumor (3)