Protein | Gene Symbol | All allelic disease phenotypes - locus/disease symbols |
| fibroblast growth factor 14 | |  | Spinocerebellar ataxia 27 -SCA27
|
|
filamin A, alpha (actin binding protein 280) | |  | MYXOMATOUS VALVULAR DYSTROPHY, X-LINKED -XMVD
|  | cardiac valvular dysplasia, x-linked -CVD1
|
| filamin C, gamma (actin-binding protein - 280) | |  | Filaminopathy, autosomal dominant -MYFM
|  | Myopathy, myofibrillar, filamin C-related -MYFM
|  | Filamin C-related -MFM
|
| four and a half LIM domain 1 | |  | reducing body myopathy -
|  | scapuloperoneal myopathy -XPMD
|  | x-linked myopathy with postural muscle atrophy -XMPMA
|  | Emery-dreifuss muscular dystrophy 6 -EDMD6
|
| frataxin | |  | Friedreich ataxia -FRDA
|  | Friedreich ataxia with retained reflexes -FARR
|
| fukutin | |  | Walker-Warburg syndrome -WWS
|  | Muscular dystrophy, Fukuyama congenital -FCMD
|  | Muscular dystrophy, limb-girdle, type 2L -LGMD2L
|  | cardiomyopathy, dilated, 1x -CMD1X
|
| | |  | walker-warburg syndrome -WWS
|  | fukuyama congenital muscular dystrophy -FCMD
|  | limb-girdle, muscular dystrophy, type 2m -LGMD2M
|
| fukutin-related protein | |  | Walker-Warburg syndrome -WWS3
|  | Muscle-eye-brain disease -MEB
|  | Muscular dystrophy, congenital, 1C -MDC1C
|  | Muscular dystrophy, limb-girdle, type 2I -LGMD2I
|
| fusion (involved in t(12;16) in malignant liposarcoma) | |  | Amyotrophic lateral sclerosis -ALS6
|
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