Protein | Gene Symbol | All allelic disease phenotypes - locus/disease symbols |
| fatty acid 2-hydroxylase | |  * Spastic paraplegia 35, autosomal recessive - SPG35 (15.35)
* Dysmyelinating leukodystrophy - FAHN (15.35)
|
fibroblast growth factor 14 | | * Spinocerebellar ataxia 27 - SCA27 (13.25)
| Fibulin 5 (extra-cellular matrix) | | * Charcot-Marie-Tooth neuropathy, with fibulin defect - (14.10)
| filamin A, alpha (actin binding protein 280) | | * Myxomatous valvular dystrophy, X-ninked - XMVD (10.71)
* cardiac valvular dysplasia, x-linked - CVD1 (10.71)
| filamin C, gamma (actin-binding protein - 280) | | * Myopathy, myofibrillar, filamin C-related - MFM5 (4.16, 5.8)
* Myopathy, distal, 4 - MPD4 (4.16, 5.8)
| four and a half LIM domain 1 | | * Scapuloperoneal myopathy - XPMD (1.3, 2.15, 5.18, 5.19, 5.20)
* Emery-dreifuss muscular dystrophy 6 - EDMD6 (1.3, 2.15, 5.18, 5.19, 5.20)
* X-linked myopathy with postural muscle atrophy - XMPMA (1.3, 2.15, 5.18, 5.19, 5.20)
* Myopathy, reducing body, X-linked, severe early-onset - (1.3, 2.15, 5.18, 5.19, 5.20)
* Myopathy, reducing body, X-linked, childhood-onset - (1.3, 2.15, 5.18, 5.19, 5.20)
* rigid spine muscular dystrophy 1 - RSMD1 (1.3, 2.15, 5.18, 5.19, 5.20)
| frataxin | | * Friedreich ataxia - FRDA (13.36)
* Friedreich ataxia with retained reflexes - FARR (13.36)
| fukutin | | * Walker-warburg syndrome - WWS (1.31, 2.5, 2.6, 10.53)
* fukuyama congenital muscular dystrophy - FCMD (1.31, 2.5, 2.6, 10.53)
* Limb-girdle, muscular dystrophy, type 2m - LGMD2M (1.31, 2.5, 2.6, 10.53)
| fukutin-related protein | | * Walker-Warburg syndrome - WWS3 (1.27, 2.3, 2.9, 2.12)
* Muscle-eye-brain disease - MEB (1.27, 2.3, 2.9, 2.12)
* Muscular dystrophy, congenital, 1C - MDC1C (1.27, 2.3, 2.9, 2.12)
* Muscular dystrophy, limb-girdle, type 2I - LGMD2I (1.27, 2.3, 2.9, 2.12)
| fusion (involved in t(12;16) in malignant liposarcoma) | | * Amyotrophic lateral sclerosis - ALS6 (12.27)
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