Diseases List
 
 
DiagnosisOmim NumberSample Count
FABRY DISEASE30150011
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1158900108
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; TYPE UNKNOWN (FSHD)1589001
FACTOR V DEFICIENCY2274002
FACTOR VII DEFICIENCY2275001
FACTOR X DEFICIENCY2276001
FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP117510043
FAMILIAL CANCER 4
FAMILIAL MULTIPLE CONGENITAL ANOMALIES - UNKNOWN SYNDROME OR INHERITANCE 1
FAMILIAL OPTIC ATROPHY; TYPE UNKNOWN; LEBER-LIKE OPTIC ATROPHY 1
FANCONI ANEMIA COMPLEMENTATION GROUP UNDETERMINED 7
FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA60713912
FANCONI ANEMIA, COMPLEMENTATION GROUP B 1
FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC22764510
FANCONI ANEMIA, COMPLEMENTATION GROUP D1; FANCD16057241
FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD22276463
FANCONI ANEMIA, COMPLEMENTATION GROUP F; FANCF6034671
FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG 2
FARBER LIPOGRANULOMATOSIS22800012
FELINE EHLERS-DANLOS SYNDROME: TYPE UNCLASSIFIED 1
FEMORAL DUPLICATION 1
FETAL AKINESIA DEFORMATION SEQUENCE; FADS2081501
FIBROBLAST GROWTH FACTOR RECEPTOR 3; FGFR31349341
FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP1351002
FIBROMUSCULAR DYSPLASIA OF ARTERIES13558029
FOCAL DYSTONIA 2159
FRAGILE SITE 10Q251366202
FRAGILE SITE 2Q13 1
FRAGILE X MENTAL RETARDATION SYNDROME30062489
FRASER SYNDROME2190003
FRIEDREICH ATAXIA 1
FRIEDREICH ATAXIA 1; FRDA22930056
FRONTONASAL DYSPLASIA1367601
FRONTOTEMPORAL DEGENERATION6002745
FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY2297002
FRYNS SYNDROME; FRNS2298503
FUCOSIDOSIS23000012
FUCOSYLTRANSFERASE 1; FUT12111001
FUMARATE HYDRATASE; FH1368501