|
101
|
|
|
FA complementation group G |
FAG, XRCC9 |
|
|
102
|
|
|
Fibroblast activation protein alpha |
DPPIV, FAPA, FAPalpha, SIMP |
Ankylosing spondylitis, Eczema, Autoimmune disease, Coronary artery disease, Crohn disease, Hypothyroidism, Inflammatory bowel disease, Inflammatory skin disease, Psoriasis, Psoriasis vulgaris, Psoriatic arthritis, Sclerosing cholangitis, Scoliosis, Systemic lupus erythematosus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Ulcerative colitis, VitiligoView all (3 more) |
|
103
|
|
|
Fibulin 1 |
FBLN, FIBL1 |
|
|
104
|
|
|
Phenylalanyl-tRNA synthetase subunit alpha |
CML33, FARSL, FARSLA, FRSA, PheHA, RILDBC2 |
|
|
105
|
|
|
Fatty acid synthase |
FAS, OA-519, SDR27X1 |
Autism, Breast neoplasm, Hepatocellular carcinoma, Cardiomyopathy, Developmental and epileptic encephalopathy, Esophageal squamous cell carcinoma, Esotropia, Hearing impairment, Heart failure, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Kidney failure, Liposarcoma, Major depressive disorder, Melanoma, Metabolic syndrome, Neurodevelopmental disorders, Obesity, Ovarian neoplasm, Parkinson disease, Depression, Diabetes mellitus, type 2View all (7 more) |
|
106
|
|
|
FAT atypical cadherin 1 |
CDHF7, CDHR8, FAT, ME5, hFat1 |
Alzheimer disease, Attention deficit hyperactivity disorder, Cerebellar ataxia, Breast cancer, Adenoid cystic carcinoma, Non-small-cell lung carcinoma, Colorectal neoplasm, Congenital esophageal anomaly, Esophageal squamous cell carcinoma, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Glioblastoma, Gout, Head and neck neoplasm, Hypertension, Liver cirrhosis, Major depressive disorder, Myasthenic syndrome, Nephrotic syndrome, Obesity, Prostate cancer, Salivary gland neoplasmsView all (7 more) |
|
107
|
|
|
FAT atypical cadherin 2 |
CDHF8, CDHR9, HFAT2, MEGF1, SCA45 |
|
|
108
|
|
|
Fibulin 2 |
- |
|
|
109
|
|
|
Fibrillin 1 |
ACMICD, ECTOL1, FBN, GPHYSD2, MASS, MFLS, MFS1, OCTD, SGS, SSKS, WMS, WMS2 |
Acromesomelic dysplasia, Aneurysm, Aortic aneurysm, Aortic rupture, Aortic valve disease, Arachnodactyly, Arthrogryposis-renal dysfunction-cholestasis syndrome, Brain aneurysm, Breast cancer, Brugada syndrome, Byzanthine arch palate, Cardiomyopathy, Color vision deficiency, Colorectal cancer, Congenital aneurysm of ascending aorta, Congenital cataract, Congenital contractural arachnodactyly, Connective tissue disease, Coronary artery disease, Craniosynostosis, Crest syndrome, Crst syndrome, Desbuquois syndrome, Ectopia lentis, Ehlers-danlos syndrome, Endometriosis, Thoracic aortic aneurysm and aortic dissection, Geleophysic dysplasia, Heart disease, Hyperglycemia, Hyperinsulinism, Left ventricular disease, Liver cirrhosis, Loeys-dietz syndrome, Marfan syndrome, Metaphyseal chondrodysplasia, Mitral valve prolapse, Mixed connective tissue disease, Myopathy, Myopia, Perrault syndrome, Pulmonary arterial hypertension, Ruptured abdominal aortic aneurysm, Ruptured aortic aneurysm, Ruptured thoracic aortic aneurysm, Scoliosis, Shprintzen-goldberg syndrome, Systemic sclerosis, Weill-marchesani syndromeView all (34 more) |
|
110
|
|
|
Fibrillin 2 |
CCA, DA9, EOMD |
Alzheimer disease, Aortic aneurysm, Autism, Brain aneurysm, Breast cancer, Cardiomyopathy, Cardiovascular disease, Carpal tunnel syndrome, Colorectal neoplasm, Congenital contractural arachnodactyly, Connective tissue disease, Coronary artery disease, Craniosynostosis, Desbuquois syndrome, Ehlers-danlos syndrome, Thoracic aortic aneurysm and aortic dissection, Global developmental delay, Hypertension, Loeys-dietz syndrome, Macular degeneration, Marfan syndrome, Migraine, Multiple system atrophy, Myocardial infarction, Myopathy, Obesity, Ocular sarcoidosis, Osteoarthritis, Pelvic organ prolapse, Pena-shokeir syndrome type i, Potassium deficiency, Psoriasis, Scoliosis, Myopia, Strabismus, Systemic lupus erythematosus, Uterine prolapse, Ventricular septal defectView all (23 more) |
