1411
|
|
|
FUT8 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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1412
|
|
|
Fucosyltransferase 9 |
Fuc-TIX |
Curated: Colorectal cancer, Diabetic neuropathy, Migraine, Schizophrenia
Unreviewed: Adenocarcinoma Of Colon, Colorectal Cancer, Liver carcinoma, Lung Cancer, Lung carcinoma, Malignant Neoplasm, Neoplasms, Sarcoidosis
|
1413
|
|
|
Fuzzy planar cell polarity protein |
CPLANE3, FY, NTD |
Curated: Caudal regression syndrome, Desbuquois syndrome, Jeune thoracic dystrophy, Majewski syndrome, Neural tube defect, Neural tube defects, x-linked, Neural tube defects, susceptibility to
Unreviewed: Acrania, Ambiguous Genitalia, Androgen-Insensitivity Syndrome, Anencephaly, Arnold-Chiari malformation, Arrhinencephaly, Autism Spectrum Disorder, Benign Prostatic Hyperplasia, Bowel incontinence, Carcinogenesis, Cataract, Caudal regression sequence, Cervical spina bifida aperta, Cervical spina bifida cystica, Cervicothoracic Spina Bifida, Chiari malformation, Ciliopathy, Congenital cataract, Congenital Cerebral Hernia, Congenital Clubfoot, Craniorachischisis, Cryptorchidism, Diastematomyelia, Double Ureter, Ectopic kidney, Encephalocele, Hermansky-Pudlak Syndrome, Hydrocephalus, Hyperparathyroidism-Jaw Tumor Syndrome, Hypertension, Hyperuricemia, Imperforate anus, Kidney disease, Lipoma, Lumbosacral Spina Bifida Aperta, Lumbosacral Spina Bifida Cystica, Lung carcinoma, Majewski Syndrome, Meningomyelocele, Multiple Lipomata, Neoplasms, Neural Tube Defect, Neurenteric Cyst, Obesity, Oral cleft, Primary Tethered cord syndrome, Pulmonary hypoplasia, Renal agenesis, Renal Insufficiency, Sacral Agenesis, Scoliosis, Spina Bifida, Spina Bifida Cystica, Spina bifida occulta, Spinal Cord Myelodysplasia, Squamous cell carcinoma, Thoracolumbosacral spina bifida aperta, Thoracolumbosacral spina bifida cystica, Tuberous Sclerosis, Upper Thoracic Spina Bifida Aperta, Upper Thoracic Spina Bifida Cystica, Urinary tract infection, Vesicoureteral Reflux
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1414
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
1415
|
|
|
Frataxin |
CyaY, FA, FARR, FRDA, X25 |
Curated: Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Diabetes mellitus type 2, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Hypertrophic cardiomyopathy, Lung cancer, Major depressive disorder, Migraine, Nonalcoholic fatty liver disease, Non-hodgkins lymphoma, Obesity, Ovarian cancer, Ovarian serous carcinoma, Pancreatic cancer, Prostate cancer, Squamous cell carcinoma, friedreich ataxia
Unreviewed: Adamantinous Craniopharyngioma, Adenocarcinoma Of Colon, Amyotrophic Lateral Sclerosis, Anemia, Ataxia, Ataxia Telangiectasia, Ataxia-oculomotor apraxia, beta Thalassemia, Bloom Syndrome, Brain Neoplasms, Bulbospinal Atrophy, X-Linked, Carcinogenesis, Cardiomyopathy, Cataract, Catecholaminergic polymorphic ventricular tachycardia, Cerebellar Ataxia, Cerebellar atrophy, Cerebellar Diseases, Ceruloplasmin deficiency, Cervical spinal cord atrophy, Charcot-Marie-Tooth Disease, Chromosomal instability, Colon Carcinoma, Colonic Neoplasms, Cone-rod dystrophy, Congenital Atransferrinemia, Congenital disorder of glycosylation, Congenital heart defects, Congenital Heart Disease, Congestive Heart Failure, Coronary Heart Disease, Degenerative Brain Disorder, Dementia, Demyelinating diseases, Dentatorubral Pallidoluysian Atrophy, Diabetes, Diabetes Mellitus, Dysarthria, Dysphagia, Epileptic encephalopathy, Esophageal neoplasm, Eye abnormalities, Fanconi Anemia, Fatigue syndrome, Fragile X Syndrome, Friedreich Ataxia, Glioma, Glycogen storage disease, Heart Diseases, Heart Failure, Hemochromatosis, Henoch-Schonlein Nephritis, Hepatocellular adenoma, Hepatolenticular Degeneration, Hereditary Hemochromatosis, Hereditary Leber Optic Atrophy, Hereditary Motor And Sensory Neuropathy With Optic Atrophy, Hereditary sensory and autonomic neuropathy, Heredodegenerative Disorders, Nervous System, Huntington Disease, Hyperbilirubinemia, Hyperlipoproteinemia, Hypertension, Hypoalbuminemia, Hypoplastic Left Heart Syndrome, Hypoxia, Impaired Cognition, Inborn Errors Of Metabolism, Iron Overload, Left Ventricular Hypertrophy, Leigh Syndrome, LEOPARD Syndrome, Leukemia, Limb-Girdle Muscular Dystrophy, Liver carcinoma, Liver neoplasms, Long QT Syndrome, Machado-Joseph Disease, Malignant Neoplasm, Marfan Syndrome, Metabolic Diseases, Metabolic syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial myopathy, Mitochondrial Respiratory Chain Deficiencies, Multiple Sclerosis, Myocardial Infarction, Myopathy, Myotonic dystrophy, Narcolepsy, Neoplasms, Nephropathy with Pretibial Epidermolysis Bullosa and Deafness, Nervous system disease, Nervous System Diseases, Nervous System Disorder, Neuroblastoma, Neurodegenerative disorder, Neurodegenerative Disorders, Neuroferritinopathy, Neuromuscular Diseases, Neuronal Ceroid Lipofuscinosis, Neuropathy, Nystagmus, Oligodendroglioma, Olivopontocerebellar Atrophies, Optic Atrophy, Optic Atrophy With Or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, And Neuropathy, Osteosarcoma, Paraparesis, Parkinson disease, Paroxysmal atrial fibrillation, Peripheral Neuropathy, Pulmonary hypertension, Pyogenic Arthritis, Pyoderma Gangrenosum And Acne, Renal cell carcinoma, Restless Legs Syndrome, Roussy-Levy Syndrome, Schizophrenia, Scoliosis, Senile Cardiac Amyloidosis, Sensory neuropathy, Sideroblastic Anemia, Sideroblastic Anemia, X-Linked, Spastic Ataxia, Spastic paraplegia, Spinocerebellar Ataxia, Spinocerebellar Degeneration, Stroke, Ventricular Septal Hypertrophy, Vitamin E Deficiency
|
1416
|
|
|
Frataxin pseudogene 1 |
FRDAP |
Curated: N/A
Unreviewed: N/A
|
1417
|
|
|
Frataxin pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
1418
|
|
|
FMR1 autosomal homolog 1 |
CMYO9A, CMYO9B, CMYP9A, CMYP9B, FXR1P, MYOPMIL, MYORIBF |
Curated: Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Congenital myopathy, Eating disorder, Gross motor development delay, Insomnia, Intellectual developmental disorder, Mastocytosis, Obesity, Schizophrenia, Scoliosis, Substance abuse, Diabetes mellitus type 2
Unreviewed: Adenocarcinoma, Amyloidosis, Amyotrophic lateral sclerosis, Anxiety Disorder, Bipolar Disorder, Brain disease, Breast Cancer, Carcinogenesis, Carcinoma, Carcinoma Of The Head And Neck, Cardiomyopathy, Cardiovascular abnormalities, Colorectal Cancer, Colorectal neoplasm, Congenital heart defects, Eating Disorders, Epilepsy, Facioscapulohumeral Muscular Dystrophy, Fragile X Syndrome, Heart Diseases, Hepatocellular carcinoma, Leukemia, Lung carcinoma, Major depressive disorder, Malignant Neoplasm, Manic Disorder, Melanoma, Mental Depression, Mental Disorders, Mental retardation, Minicore myopathy with external ophthalmoplegia, Miscarriage, Mood Disorder, Mouth neoplasm, Myopathy, Myotonia congenita, Neoplasm, Neoplasms, Nephroblastoma, Ovarian neoplasm, Periapical Periodontitis, Prostate cancer, Rhabdomyosarcoma, Squamous cell carcinoma, Triple negative breast cancer, Triple Negative Breast Neoplasms, Urinary bladder neoplasms, Ventricular tachycardia, Wilms tumor
|
1419
|
|
|
FMR1 autosomal homolog 2 |
FMR1L2, FXR2P |
Curated: Atrial fibrillation, Atrial flutter
Unreviewed: Amyotrophic lateral sclerosis, Breast neoplasm, Down Syndrome, Fragile X Syndrome, Megakaryocytic Leukemia, Mental retardation
|
1420
|
|
|
FXYD domain containing ion transport regulator 1 |
PLM |
Curated: Schizophrenia
Unreviewed: Alzheimer disease, Aortic Valve Insufficiency, Arthritis, Cardiomyopathy, Chronic obstructive pulmonary disease, Colorectal Cancer, Colorectal neoplasm, Congestive Heart Failure, Coronary Arteriosclerosis, Heart Failure, Hirschsprung Disease, Hypokalemic Periodic Paralysis, Imperforate anus, Myocardial Ischemia, Osteoglosphonic dysplasia, Parkinson disease, Quadriplegia, Respiratory Distress Syndrome, Restless Legs Syndrome, Rett Syndrome, Sleep Apnea, Stress Disorder, Stroke
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