901
|
|
|
FKBP6 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
902
|
|
|
FKBP prolyl isomerase 7 |
FKBP23, PPIase |
Curated: N/A
Unreviewed: Atrial fibrillation, Lateral Sclerosis, Malignant Neoplasm, Neoplasms, Parkinson disease, Prostate cancer, Stomach Diseases
|
903
|
|
|
FKBP prolyl isomerase 8 |
FKBP38, FKBPr38 |
Curated: Alzheimer disease, Attention deficit hyperactivity disorder, Breast cancer, Crohn disease, Gastroesophageal reflux disease, Inflammatory bowel disease, Substance abuse
Unreviewed: Hepatocellular carcinoma, Lateral Sclerosis, Long qt syndrome, Neural Tube Defect, Neuroblastoma, Spina Bifida
|
904
|
|
|
FKBP8 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
905
|
|
|
FKBP prolyl isomerase 9 |
FKBP60, FKBP63, PPIase |
Curated: Schizophrenia
Unreviewed: Breast neoplasm, Glioblastoma, Lateral Sclerosis, Malignant Neoplasm, Parkinson disease, Prostate cancer, Stomach Diseases
|
906
|
|
|
FKBP prolyl isomerase 9 pseudogene 1 |
FKBP9L |
Curated: N/A
Unreviewed: Squamous cell carcinoma
|
907
|
|
|
FKBP prolyl isomerase like |
DIR1, NG7, WISP39 |
Curated: Alzheimer disease, Breast neoplasms, Interstitial cystitis, Hypothyroidism, Inflammatory bowel disease, Membranous glomerulonephritis, Nephrolithiasis, Psoriasis, Rheumatoid arthritis, Systemic lupus erythematosus
Unreviewed: Age-related macular degeneration, Azoospermia, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Diabetes mellitus, Diabetes mellitus, type 1, Endometrial hyperplasia, Endometrioid carcinoma, Gestational diabetes, Glycogen Storage Disease, Hereditary breast and ovarian cancer syndrome, Lung Cancer, Lung carcinoma, Lung Neoplasms, Macular degeneration, Male infertility, Malignant Neoplasm, Mammary Neoplasms, Marfan Syndrome, Neoplasms, Non-obstructive azoospermia, Oestrogen Receptor Positive Breast Cancer, Renal cell carcinoma
|
908
|
|
|
Fukutin related protein |
FKTR, LGMD2I, LGMDR9, MDC1C, MDDGA5, MDDGB5, MDDGC5 |
Curated: Limb girdle muscular dystrophy, Dilated cardiomyopathy, Congenital muscular dystrophy due to dystroglycanopathy, Congenital muscular dystrophy, Congenital myopathy, Muscle eye brain disease, Muscular dystrophy, Myopathy, Distal hereditary motor neuropathy, Paresthesia, Diabetes mellitus type 1, Diabetes mellitus type 2, Walker-warburg syndrome, myopathy caused by variation in FKRP
Unreviewed: Absence Of Septum Pellucidum, Acquired Kyphoscoliosis, Agenesis Of Corpus Callosum, Agyria, alpha-Dystroglycanopathy, Amyotrophy, Anterior segment dysgenesis, Arachnodactyly, Becker Muscular Dystrophy, Bethlem Myopathy, Brain disease, Brain malformation, Campomelic Dysplasia, Cardiomyopathy, Cataract, Cerebellar atrophy, Cerebellar Hypoplasia, Cerebral cortical atrophy, Cobblestone Lissencephaly, Congenital Coloboma Of Iris, Congenital contracture, Congenital heart defects, Congenital Hypoplasia Of Penis, Congenital Keratoglobus, Congenital kyphoscoliosis, Congenital Meningocele, Congenital Muscular Dystrophy With Cerebellar Involvement, Congenital Muscular Dystrophy With Intellectual Disability, Congenital Muscular Dystrophy Without Intellectual Disability, Congenital ocular coloboma, Congestive Heart Failure, Contracture, Craniometaphyseal Dysplasia, Cryptorchidism, Cyst, Dandy-Walker Syndrome, Developmental Delay, Diabetes Mellitus, Diabetes mellitus, type 1, Distal myopathy, Drachtman Weinblatt Sitarz syndrome, Duchenne muscular dystrophy, Edema, Facial paralysis, Fukuyama Type Congenital Muscular Dystrophy, Glaucoma, Glaucoma, congenital, Glycogen storage disease, Heart disease, Heart Failure, Hemiplegia/hemiparesis, Holoprosencephaly, Hydrocephalus, Hypertrophy, Hypoplasia Of Corpus Callosum, Hypoplasia Of The Optic Nerve, Hypotonia, Impaired Cognition, Imperforate anus, Intellectual developmental disorder, Language development disorders, Left Ventricular Hypertrophy, Limb-girdle muscle atrophy, Limb-Girdle Muscular Dystrophy, Limb-Girdle Muscular Dystrophy-Dystroglycanopathy, Lymphocytic Leukemia, Macrocephaly, Macroglossia, Meningoencephalocele, Mental retardation, Microcephaly, Microcornea, Microphthalmos, Microtia, Motor delay, Muscle Eye Brain Disease, Muscular Dystrophy-Dystroglycanopathy, Myasthenic syndrome, Myopia, Myositis, Nasopharyngeal Carcinoma, Necrotizing myopathy, Neurodegenerative disorder, Neuromuscular Diseases, Neuronal Heterotopia, Occipital Encephalocele, Optic Atrophy, Pachygyria, Pancreatitis, Penis Agenesis, Polymicrogyria, Posteriorly Rotated Ear, Renal dysplasia, Respiratory Failure, Retinal Detachment, Retinal Dysplasia, Retinal Dystrophy, Retinitis Pigmentosa, Rhabdomyolysis, Sarcoglycanopathy, Sarcotubular myopathy, Scoliosis, Specific Learning Disorder, Speech Disorders, Strabismus, Submucosal cleft palate, Syndromic microphthalmia, Ventricular tachycardia, Walker-Warburg Congenital Muscular Dystrophy, Walker-Warburg Syndrome
|
909
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
910
|
|
|
- |
FKSG52, FKSG55, FKSG56, FKSG57, FKSG60, FKSG61, FKSG64, FKSG65, FKSG66, FKSG67, FKSG68, FKSG70 |
Curated: N/A
Unreviewed: N/A
|