4741
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Fukutin related protein |
FKTR, LGMD2I, LGMDR9, MDC1C, MDDGA5, MDDGB5, MDDGC5 |
Limb girdle muscular dystrophy, Dilated cardiomyopathy, Congenital muscular dystrophy due to dystroglycanopathy, Congenital muscular dystrophy, Congenital myopathy, Limb-girdle muscular dystrophy, Muscle eye brain disease, Muscular dystrophy, Myopathy, Distal hereditary motor neuropathy, Paresthesia, Diabetes mellitus type 1, Diabetes mellitus type 2, Walker-warburg syndrome |
4742
|
|
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Fukutin |
CMD1X, FCMD, LGMD2M, LGMDR13, MDDGA4, MDDGB4, MDDGC4 |
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4743
|
|
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Flagellum associated containing coiled-coil domains 1 |
ALS2CR12 |
Anterior uveitis, Basal cell carcinoma, Skin neoplasms, Breast cancer, Breast neoplasms, Cancer, Lymphocytic leukemia, Colorectal cancer, Melanoma, Cutaneous squamous cell carcinoma, Esophageal cancer, Esophageal squamous cell carcinoma, Estrogen-receptor negative breast cancer, Keratinocyte carcinoma, Lung cancer, Melanocytic nevus, Non-small cell lung carcinoma, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Rheumatoid arthritis, Seborrheic keratosis, Skin cancer, Skin disease, Squamous cell carcinomaView all (10 more) |
4744
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|
|
Flavin adenine dinucleotide synthetase 1 |
FAD1, FADS, LSMFLAD, PP591 |
|
4745
|
|
|
Folliculin |
BHD, DENND8B, FLCL |
|
4746
|
|
|
Filaggrin |
ATOD2, FLG-1, FLG1 |
Asthma, Eczema, Ichthyosis vulgaris, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Contact dermatitis, Dermatitis, Atopic dermatitis, Dermatomycosis, Dermatophytosis, Ichthyosis, Insomnia, Respiratory system disease, Sebaceous gland disease, Skin disease |
4747
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|
|
Filaggrin 2 |
IFPS, PSS6 |
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4748
|
|
|
Fli-1 proto-oncogene, ETS transcription factor |
BDPLT21, EWSR2, FLI-1, SIC-1 |
Autoimmune thrombocytopenic purpura, Platelet-type bleeding disorder, Platelet disorder, Lymphocytic leukemia, Congenital left-sided heart lesions, Corneal astigmatism, Extraskeletal ewing sarcoma, Iga nephropathy, Liver cirrhosis, Medulloblastoma, Multiple sclerosis, Open angle glaucoma, Paris-trousseau thrombocytopenia, Peripheral primitive neuroectodermal tumor, Rheumatoid arthritis, Sarcoma, Skeletal ewing sarcoma, Systemic lupus erythematosus, Thrombocytopenia, Diabetes mellitus type 1, Diabetes mellitus type 2, VitiligoView all (7 more) |
4749
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|
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FLII actin remodeling protein |
CMD2J, FLI, FLIL, Fli1 |
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4750
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|
|
Filamin A |
ABP-280, ABPX, CSBS, CVD1, FGS2, FLN, FLN-A, FLN1, FMD, MNS, NHBP, OPD, OPD1, OPD2, XLVD, XMVD |
Ambiguous genitalia, Aortic aneurysm, Breast neoplasms, Cardiac valvular dysplasia, Conductive hearing loss, Congenital cartilage disorder, Congenital heart defects, Congenital idiopathic intestinal pseudoobstruction, Congenital omphalocele, Congenital short bowel syndrome, Connective tissue disease, Craniosynostosis, Desbuquois syndrome, Developmental delay, Dysgenesis of corpus callosum, Developmental and epileptic encephalopathy, Ehlers-danlos syndrome, Epilepsy, Thoracic aortic aneurysm and aortic dissection, Frontometaphyseal dysplasia, Global developmental delay, Hearing impairment, Periventricular nodular heterotopia, Hydronephrosis, Intellectual developmental disorder, Intestinal obstruction, Liver cirrhosis, Marfan syndrome, Migraine, Mitral valve prolapse, Myopia, Neurodevelopmental disorder, Nonalcoholic fatty liver disease, Orofacial cleft, Osteochondrodysplasias, Otopalatodigital spectrum disorder, Otopalatodigital syndrome, Patent ductus arteriosus, Periventricular heterotopia, x-linked, Scoliosis, Intellectual disability, Terminal osseous dysplasia with pigmentary defects, Tetralogy of fallot, Thrombocytopenia, Uranostaphyloschisis, Ventricular septal defect, Wolff-parkinson-white syndrome, X-linked ehlers-danlos syndrome, X-linked keloid scarring syndromeView all (34 more) |
