Clinical Trials Involving Rare Diseases: F
- FACES Syndrome (4)
- FMR1-related Primary Ovarian Insufficiency (3)
- FOXG1 Syndrome (1)
- Fabry Disease (198)
- Facioscapulohumeral Muscular Dystrophy (51)
- Factor V Deficiency (1)
- Factor VII Deficiency (7)
- Factor X Deficiency (4)
- Factor XI Deficiency (3)
- Factor XII Deficiency (1)
- Factor XIII Deficiency (12)
- Fallopian Tube Cancer (728)
- Familial Adenomatous Polyposis (79)
- Familial Alzheimer Disease (3,025)
- 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 (11)
- Familial Hypertrophic Cardiomyopathy (6)
- Familial Hypobetalipoproteinemia (11)
- 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 (26)
- Familial Mediterranean Fever (162)
- Familial Multiple Lipomatosis (1)
- Familial Pancreatic Cancer (18)
- Familial Partial Lipodystrophy (10)
- Familial Partial Lipodystrophy Type 2 (6)
- Familial Porencephaly (1)
- Familial Prostate Cancer (7)
- Familial Thoracic Aortic Aneurysm and Aortic Dissection (3)
- Familial Thyroglossal Duct Cyst (1)
- Familial Transthyretin Amyloidosis (83)
- Familial Tumoral Calcinosis (1)
- Fanconi Anemia (99)
- Fanconi Bickel Syndrome (1)
- Fanconi Syndrome (108)
- Farber Disease (2)
- Fascioliasis (2)
- Fatal Familial Insomnia (7)
- Fatty Acid Hydroxylase-associated Neurodegeneration (1)
- Felty's Syndrome (1)
- Femur Fibula Ulna Syndrome (1)
- Fetal Macrosomia (22)
- Fetal Thalidomide Syndrome (8)
- Fetal and Neonatal Alloimmune Thrombocytopenia (4)
- Fibrillary Glomerulonephritis (2)
- Fibrinogen Deficiency, Congenital (9)
- Fibrodysplasia Ossificans Progressiva (19)
- Fibrolamellar Carcinoma (16)
- Fibrosarcoma (123)
- Fibrous Dysplasia (28)
- Florid Cemento-osseous Dysplasia (1)
- Focal Cortical Dysplasia of Taylor (2)
- Focal Dermal Hypoplasia (5)
- Focal Segmental Glomerulosclerosis (91)
- Focal Task-specific Dystonia (54)
- Follicular Lymphoma (1,322)
- 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 (82)
- Frontal Fibrosing Alopecia (10)
- Frontotemporal Dementia (256)
- Frontotemporal Dementia, Ubiquitin-positive (256)
- Fructose-1,6-bisphosphatase Deficiency (1)
- Fryns Syndrome (1)
- Fucosidosis (9)
- Fumarase Deficiency (2)
- Functioning Pancreatic Endocrine Tumor (3)