4551
|
|
|
Fas binding factor 1 |
Alb, FBF-1 |
|
4552
|
|
|
F-box DNA helicase 1 |
FBXO18, Fbx18, hFBH1 |
|
4553
|
|
|
Fibrillarin |
FIB, FLRN, Nop1, RNU3IP1 |
|
4554
|
|
|
Fibulin 1 |
FBLN, FIBL1 |
|
4555
|
|
|
Fibulin 2 |
- |
|
4556
|
|
|
Fibulin 5 |
ADCL2, ARCL1A, ARMD3, CMT1H, DANCE, EVEC, FIBL-5, HNARMD, UP50 |
Cutis laxa, Central nervous system cancer, Charcot-marie-tooth disease, Accessory skin tag, Congestive heart failure, Demyelinating hereditary motor and sensory neuropathy, Emphysema, Essential tremor, Benign pemphigus, Glioblastoma, Glioma, Heart failure, Pulmonary hypertension, Darier disease, Age-related macular degeneration, Major depressive disorder, Optic atrophy, Prostatic neoplasms, Proximal spinal muscular atrophy, Respiratory system infectious disease, Rothmund-thomson syndrome, Vascular diseaseView all (7 more) |
4557
|
|
|
Fibulin 7 |
TM14 |
|
4558
|
|
|
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, Dilated cardiomyopathy, Color vision deficiency, Colorectal cancer, Congenital aneurysm of ascending aorta, Congenital cataract, Congenital contractural arachnodactyly, Congenital diaphragmatic hernia, Congenital pectus carinatum, Congenital scoliosis, Connective tissue disease, Coronary artery disease, Craniosynostosis, Crest syndrome, Crst syndrome, Desbuquois syndrome, Dilatation of pulmonary artery, Dissecting aortic aneurysm, Dissection of aorta, 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, Tetralogy of fallot, Thoracic aortic aneurysm, Thoracoabdominal aortic aneurysm, Weill-marchesani syndromeView all (43 more) |
4559
|
|
|
Fibrillin 2 |
CCA, DA9, EOMD |
Alzheimer disease, Aortic aneurysm, Autism, Brain aneurysm, Breast cancer, Dilated cardiomyopathy, Cardiovascular disease, Carpal tunnel syndrome, Colorectal neoplasms, 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 , Potassium deficiency, Psoriasis, Scoliosis, Myopia, Strabismus, Systemic lupus erythematosus, Tetralogy of fallot, Uterine prolapse, Ventricular septal defectView all (24 more) |
4560
|
|
|
Fibrillin 3 |
- |
|
