F – Index Rare Diseases & Conditions

Fabry Disease
Facioscapulohumeral Muscular Dystrophy
Factor VII Deficiency
Factor X Deficiency
Factor XI Deficiency
Factor XII Deficiency
Factor XIII Deficiency
Familial Adenomatous Polyposis
Familial Cold Autoinflammatory Syndrome
Familial Encephalopathy with Neuroserpin Inclusion Bodies
Familial Eosinophilic Cellulitis
Familial Hypercholesterolemia
Familial Hypophosphatemia
Familial Isolated Hypoparathyroidism
Familial Lipoprotein Lipase Deficiency
Familial Mediterranean Fever
Familial Partial Lipodystrophy
Familial Platelet Disorder with Associated Myeloid Malignancy
Fanconi Anemia
Fatal Familial Insomnia
Felty Syndrome
Femoral Facial Syndrome
Ferroportin Disease
Fetal Alcohol Syndrome
Fetal Hydantoin Syndrome
Fetal Retinoid Syndrome
Fetal Valproate Syndrome
FG Syndrome Type 1
Fibrodysplasia Ossificans Progressiva
Fibrolamellar Carcinoma
Fibromuscular Dysplasia
Fibrosing Mediastinitis
Fibrous Dysplasia
Filippi Syndrome
Fitz Hugh Curtis Syndrome
Floating Harbor Syndrome
Focal Dermal Hypoplasia
Focal Segmental Glomerulosclerosis
Follicular Lymphoma
Food Protein-Induced Enterocolitis Syndrome
Formaldehyde Poisoning
Fountain Syndrome
Fournier Gangrene
Fox Fordyce Disease
Fragile X Syndrome
Fraser Syndrome
Freeman Sheldon Syndrome
Frey Syndrome
Friedreich’s Ataxia
Froelich Syndrome
Frontofacionasal Dysplasia
Frontonasal Dysplasia
Frontotemporal Degeneration
Fructose Intolerance, Hereditary
Fryns Syndrome
Fukuyama Type Congenital Muscular Dystrophy
Functional Neurological Disorder