Clinical Trials Involving Rare Diseases: F
- FACES Syndrome (2)
- FMR1-related Primary Ovarian Insufficiency (3)
- FOXG1 Syndrome (2)
- Fabry Disease (159)
- Facioscapulohumeral Muscular Dystrophy (39)
- Factor V Deficiency (1)
- Factor VII Deficiency (5)
- Factor X Deficiency (4)
- Factor XI Deficiency (3)
- Factor XII Deficiency (1)
- Factor XIII Deficiency (12)
- Fallopian Tube Cancer (628)
- Familial Adenomatous Polyposis (59)
- Familial Alzheimer Disease (2,341)
- Familial Atrial Fibrillation (2)
- Familial Cerebral Cavernous Malformation (9)
- Familial Chylomicronemia Syndrome (10)
- Familial Cold Autoinflammatory Syndrome (18)
- Familial Colorectal Cancer (7)
- Familial Deafness (1)
- Familial Dilated Cardiomyopathy (3)
- Familial Dysautonomia (12)
- Familial Encephalopathy With Neuroserpin Inclusion Bodies (2)
- Familial Exudative Vitreoretinopathy (1)
- Familial HDL Deficiency (2)
- Familial Hemiplegic Migraine (4)
- Familial Hemophagocytic Lymphohistiocytosis (10)
- Familial Hypertrophic Cardiomyopathy (4)
- Familial Hypobetalipoproteinemia (9)
- Familial Isolated Hyperparathyroidism (2)
- Familial Isolated Pituitary Adenoma (1)
- Familial Joint Instability Syndrome (1)
- Familial Lipoprotein Lipase Deficiency (21)
- Familial Mediterranean Fever (128)
- Familial Multiple Lipomatosis (1)
- Familial Pancreatic Cancer (15)
- Familial Partial Lipodystrophy (8)
- Familial Partial Lipodystrophy Type 2 (4)
- Familial Prostate Cancer (6)
- Familial Thoracic Aortic Aneurysm and Aortic Dissection (3)
- Familial Transthyretin Amyloidosis (50)
- Familial Tumoral Calcinosis (1)
- Fanconi Anemia (89)
- Fanconi Syndrome (98)
- Farber Disease (2)
- Fascioliasis (2)
- Fatal Familial Insomnia (3)
- Felty's Syndrome (1)
- Fetal Macrosomia (40)
- Fetal Thalidomide Syndrome (5)
- Fetal and Neonatal Alloimmune Thrombocytopenia (2)
- Fibrillary Glomerulonephritis (1)
- Fibrinogen Deficiency, Congenital (9)
- Fibrodysplasia Ossificans Progressiva (10)
- Fibrolamellar Carcinoma (10)
- Fibrosarcoma (103)
- Fibrous Dysplasia (22)
- Focal Cortical Dysplasia of Taylor (2)
- Focal Dermal Hypoplasia (5)
- Focal Segmental Glomerulosclerosis (72)
- Focal Task-specific Dystonia (51)
- Follicular Lymphoma (1,182)
- Fournier Gangrene (8)
- Fowler's Syndrome (2)
- Fragile X Syndrome (76)
- Fraser Syndrome (1)
- Frasier Syndrome (2)
- Freeman Sheldon Syndrome (3)
- Frey's Syndrome (1)
- Friedreich Ataxia (64)
- Frontal Fibrosing Alopecia (8)
- Frontotemporal Dementia (185)
- Frontotemporal Dementia, Ubiquitin-positive (185)
- Fryns Syndrome (1)
- Fucosidosis (9)
- Fumarase Deficiency (1)
- Functioning Pancreatic Endocrine Tumor (3)