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231
|
|
|
Follicle stimulating hormone receptor |
FSHR1, FSHRO, LGR1, ODG1 |
46, xx gonadal dysgenesis, 46,xx gonadal dysgenesis, Arachnodactyly, Dwarfism, Enlarged polycystic ovaries, Erectile dysfunction, Gonadal dysgenesis, Microcephaly, Osteopenia, Osteoporosis, Osteoporosis of vertebrae, Sclerocystic ovaries, Ovarian hyperstimulation syndrome, Physiologic amenorrhea, Pleural effusion, Polycystic ovary syndrome, Premature menopause, Ovarian failure, Prostate cancer, Pulmonary fibrosis, Secondary physiologic amenorrhea, Streak ovary, Urogenital abnormalitiesView all (8 more) |
|
232
|
|
|
Ferritin heavy chain 1 |
FHC, FTH, FTHL6, HFE5, NBIA9, PIG15, PLIF |
Bestrophinopathy, Degenerative diseases, central nervous system, Dermatitis, Glioma, Iron overload, Malignant mesothelioma, Melancholia, Mental depression, Neurodegenerative disorders, Vitelliform macular dystrophy |
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233
|
|
|
Ferritin light chain |
FTL1, LFTD, NBIA3 |
Alopecia, Anarthria speech disorder, Arthritis, Blepharospasm, Cataract, Cavitation of the basal ganglia, Choreoathetosis, Dementia, Developmental regression, Dysarthria, Dyskinetic syndrome, Dysphagia, Genetic hyperferritinemia without iron overload, Hereditary hyperferritinemia with congenital cataracts, Heredodegenerative disorders, nervous system, Iron metabolism disorders, L-ferritin deficiency, Language disorders, Laryngeal dystonia, Orofacial dyskinesia, Spastic diplegia, Melancholia, Mental depression, Mental retardation, Mood swings, Movement disorders, Neuroferritinopathy, Nonorganic psychosis, Obesity, Optic atrophy, Osteoarthrosis deformans, Parkinson disease, Psychosis, Restless legs syndrome, Seizure, Subcortical dementia, Writer`s crampView all (22 more) |
|
234
|
|
|
Alpha-L-fucosidase 1 |
FUCA |
Angiokeratoma, Anhidrosis, Brachycephaly, Camptodactyly of fingers, Cerebral atrophy, Developmental delay, Dwarfism, Frontal bossing, Fucosidase deficiency disease, Fucosidosis, Congenital gallbladder anomaly, Hypothyroidism, Mental retardation, Lipoatrophy, Lipodystrophy, Macroglossia, Macrostomia, Pfaundler-hurler syndrome, Polyneuropathy, Scoliosis, Skin diseases, vascular, Spastic quadriplegiaView all (7 more) |
|
235
|
|
|
FUS RNA binding protein |
ALS6, ETM4, FUS1, HNRNPP2, POMP75, TLS, altFUS |
Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis with dementia, Amyotrophy, Anxiety disorder, Apraxia, Breast cancer, Bulbar palsy, Cerebellar ataxia, Dementia, Dysarthria, Dyscalculia, Dysphagia, Fibromyxosarcoma, Frontotemporal dementia, Frontotemporal dementia with motor neuron disease, Hallucinations, Hereditary essential tremor, Laryngospasm, Liposarcoma, Mental depression, Mood swings, Movement disorders, Myxofibrosarcoma, Myxoid liposarcoma, Parkinson disease, Ptosis, Respiratory failure, Sensorineural hearing loss, Sensory neuropathy, TremorView all (15 more) |
|
236
|
|
|
Fucosyltransferase 2 (H blood group) |
B12QTL1, SE, SEC2, Se2, sej |
Ankylosing spondylitis, Arthritis, Autoimmune diseases, Autoimmune thyroiditis, Cardiovascular diseases, Celiac disease, Cholangitis, Common variable immunodeficiency, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Diabetes mellitus, Ileocolitis, Inflammatory bowel disease, Lupus erythematosus, Psoriasis, Ulcerative colitisView all (2 more) |
|
237
|
|
|
Fucosyltransferase 5 |
FUC-TV |
|
|
238
|
|
|
Fucosyltransferase 6 |
FCT3A, FT1A, Fuc-TVI, FucT-VI |
|
|
239
|
|
|
Fucosyltransferase 7 |
FucT-VII |
|
|
240
|
|
|
Fucosyltransferase 8 |
CDGF, CDGF1 |
Acquired kyphoscoliosis, Congenital disorder of glycosylation with defective fucosylation, Congenital kyphoscoliosis, Developmental delay, Dwarfism, Glaucoma, congenital, High palate, Mental retardation, Microcephaly, Osteopenia, Schizophrenia |
