|
Disease
|
|
Also Known as |
|
Fabry Disease
|
 |
Anderson-Fabry Disease |
|
|
Factor II Deficiency |
|
Hypoprothrombinaemia |
|
Factor V Deficiency
|
|
Parahaemophilia |
|
Factor VII Deficiency
|
|
Extrinsic Factor Deficiency |
|
Factor VIII Deficiency
|
|
Haemophilia A |
|
Factor IX Deficiency
|
|
Haemophilia B |
|
Factor X Deficiency
|
|
Stuart Prower Disease |
|
Factor XI Deficiency
|
|
Haemophilia C |
|
Factor XII Deficiency
|
|
Hagemann Factor Deficiency |
|
|
Fahr's Disease |
|
Cerebrovascular
Ferrocalcinosis |
|
|
Familial Articular Chondrocalcinosis |
|
Familial Calcium Gout |
|
Familial Combined Hyperlipidaemia
|
|
FCHL |
|
Familial Hypertriglyceridaemia
|
|
Hyperlipoproteinaemia Type IV |
|
Familial Hypoalphalipoproteinaemia
|
|
High
Density Lipoprotein Deficiency |
|
|
Familial Juvenile Hyperuricaemic Nephropathy |
|
Familial Gouty Nephropathy |
|
Fanconi Anaemia
|
|
Congenital Pancytopenia
|
|
Fanconi Syndrome
|
|
De
Toni-Fanconi Syndrome |
|
Fanconi-Bickel Syndrome
|
|
Fanconi-Bickel Syndrome |
|
Farber Disease
|
|
Ceramidase Deficiency |
|
Fatty Acid Oxidation Disorders -General
|
|
FOD's |
|
Fibrodysplasia Ossificans Progressiva
|
|
FOP |
|
Fibrous Dysplasia - General
|
|
Idiopathic Fibrous
Hyperplasia |
|
Folinic Acid Responsive Seizures
|
|
|
|
Fragile X Syndrome
|
|
FRAXA |
|
Friedreich's Ataxia
|
|
FRDA |
|
Fructose 1, 6-Bisphosphatase Deficiency
|
|
Fructose 1, 6-Diphosphate Deficiency |
|
|
Fructose Intolerance -
Hereditary |
|
Fructosaemia |
|
|
Fructosuria |
|
Essential Fructosuria |
|
|
Fucosidosis |
|
Alpha-L-Fucosidase Deficiency |
|
|
Fukuyama Muscular
Dystrophy |
|
Cerebromuscular Dystrophy, Fukuyama Type |
|
|
Fumarase
Deficiency |
|
Fumaric Aciduria |
