911
|
|
|
Fukutin |
CMD1X, FCMD, LGMD2M, LGMDR13, MDDGA4, MDDGB4, MDDGC4 |
Curated: Limb girdle muscular dystrophy, Dilated cardiomyopathy, Cataract, Congenital muscular dystrophy, Global developmental delay, Muscle eye brain disease, Muscular dystrophy, Myocardial infarction, Walker-warburg syndrome, myopathy caused by variation in FKTN
Unreviewed: Absence Of Septum Pellucidum, Acquired Kyphoscoliosis, Agenesis Of Corpus Callosum, Agyria, alpha-Dystroglycanopathy, Amyotrophy, Anterior segment dysgenesis, Astrocytoma, Atrial Septal Defect, Bohring syndrome, Brachycephaly, Brain malformation, Breast Cancer, Bundle branch block, Campomelic Dysplasia, Cardiomyopathy, Central nervous system disease, Cerebellar atrophy, Cerebellar Hypoplasia, Cobblestone Lissencephaly, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Congenital contracture, Congenital Hypoplasia Of Penis, Congenital Keratoglobus, Congenital kyphoscoliosis, Congenital Meningocele, Congenital Muscular Dystrophy Without Intellectual Disability, Congenital ocular coloboma, Congenital Pectus Excavatum, Congestive Heart Failure, Craniometaphyseal Dysplasia, Cryptorchidism, Dandy-Walker Syndrome, Developmental Delay, Dilated Cardiomyopathy, Dolichocephaly, Duchenne Muscular Dystrophy, Dysferlinopathy, Eichsfeld type congenital muscular dystrophy, Encephalocele, Eye abnormalities, Fukuyama Type Congenital Muscular Dystrophy, Gallbladder cancer, Glaucoma, Glaucoma, congenital, Hearing Loss, Heart Failure, Hemiplegia/hemiparesis, Holoprosencephaly, Hydrocephalus, Hyperopia, Hypertrophic cardiomyopathy, Hypoplasia Of Corpus Callosum, Hypoplasia Of The Optic Nerve, Hypotonia, Impaired Cognition, Imperforate anus, Intellectual developmental disorder, Limb-girdle muscle atrophy, Limb-Girdle Muscular Dystrophy, Limb-Girdle Muscular Dystrophy-Dystroglycanopathy, Lipoatrophy, Lipodystrophy, Macrocephaly, Malignant Neoplasm, Meningoencephalocele, Mental retardation, Microcephaly, Microcornea, Microphthalmos, Microtia, Motor delay, Muscle Eye Brain Disease, Muscular Dystrophy-Dystroglycanopathy, Myopathy, Myopia, Neuromuscular disease, Neuronal Heterotopia, Occipital Encephalocele, Optic Atrophy, Pachygyria, Palmoplantar keratoderma, Plagiocephaly, Polymicrogyria, Posteriorly Rotated Ear, Primary microcephaly, Pulmonary Stenosis, Renal dysplasia, Retinal Detachment, Retinal Dysplasia, Retinal Dystrophy, Retinitis pigmentosa, Sarcoglycanopathy, Scoliosis, Specific Learning Disorder, Speech Disorders, Stomach Carcinoma, Stomach Neoplasms, Strabismus, Submucosal cleft palate, Syndromic microphthalmia, Transposition Of Great Vessels, Walker-Warburg Congenital Muscular Dystrophy, Walker-Warburg Syndrome
|
912
|
|
|
FKTN antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
913
|
|
|
- |
- |
Curated: N/A
Unreviewed: Lymphoma
|
914
|
|
|
Flagellum associated containing coiled-coil domains 1 |
ALS2CR12 |
Curated: 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 carcinoma
Unreviewed: Anthracosis, Basal Cell Neoplasm, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Esophageal neoplasm, Esophagus Neoplasm, Lung neoplasms, Mammary Neoplasms, Marfan Syndrome, Prostatic neoplasm
|
915
|
|
|
Flavin adenine dinucleotide synthetase 1 |
FAD1, FADS, LSMFLAD, PP591 |
Curated: Squamous cell carcinoma, myopathy with abnormal lipid metabolism
Unreviewed: Alzheimer disease, Asthma, Bipolar Disorder, Breast neoplasm, Carbamoyl Phosphate Synthase Deficiency, Cardiovascular Diseases, Cognitive disorder, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Dermatitis, Diabetes, Diabetes Mellitus, Dyslipidemias, Dysphagia, Eczema, Hypospadias, Impaired Cognition, Inborn Errors Of Metabolism, Inflammatory Bowel Disease, Ischemic Stroke, Lichen amyloidosis, Lipid Storage Myopathy, Malnutrition, Mental Depression, Metabolic Diseases, Metabolic Syndrome, Mitochondrial disease, Mitochondrial Respiratory Chain Deficiencies, Multiple Acyl-CoA Dehydrogenase Deficiency, Myopathy, Myopathy With Abnormal Lipid Metabolism, Neoplasms, Obesity, Pancreatic ductal carcinoma, Pancreatic neoplasm, Pena Shokeir syndrome, Penile Hypospadias, Pneumothorax, Polycystic Ovary Syndrome, Progressive Supranuclear Palsy, Prostate cancer, Stomach Carcinoma, Stomach Neoplasms
|
916
|
|
|
Folliculin |
BHD, DENND8B, FLCL |
Curated: 17p11.2 microduplication syndrome, Birt-hogg-dube syndrome, Renal cell carcinoma, Colorectal cancer, Colorectal neoplasms, Liver neoplasms, Omphalocele exstrophy imperforate anus, Potocki-lupski syndrome, Prostate cancer
Unreviewed: Adenocarcinoma, Amyotrophic Lateral Sclerosis, Angiolipoma, Apraxia, Asthma, Astrocytoma, Ataxia Telangiectasia, Autism, Birt-Hogg-Dube Syndrome, Bladder carcinoma, Blister, Brain neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bronchopulmonary Disease, Carcinogenesis, Carcinoma, Cardiovascular Abnormalities, Cerebral Cavernous Malformation, Chromophobe Carcinoma, Chronic disease, Colonic neoplasm, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Connective Tissue Disease, Cyst, Cystic lung disease, Developmental Delay, Dwarfism, Dysphasia, Dystonia, Emphysema, Endometrial carcinoma, Eosinophilia, Episodic Kinesigenic Dyskinesia, Erdheim-Chester Disease, Fibrofolliculoma, Frontotemporal dementia, Gastroesophageal Reflux Disease, Genetic predisposition to disease, Hamartoma, Hereditary Cancer Syndrome, Hereditary Leiomyomatosis and Renal Cancer, Hereditary nonpolyposis colorectal cancer, Hereditary Renal Carcinoma, High palate, Hip Dysplasia, Hyperopia, Hypertension, Hypocholesterolemia, Hypoplasia Of Corpus Callosum, Kidney Cancer, Kidney disease, Kidney Neoplasm, Language Disorders, Large intestinal polyposis, Leiomyosarcoma Of Uterus, Lipoma, Liver Cancer, Lung disease, Lung Diseases, Lung Neoplasms, Macrostomia, Malignant Neoplasm, Malocclusion, Megalencephaly, Polymicrogyria, Polydactyly, Hydrocephalus Syndrome, Mental retardation, Microcephaly, Micrognathism, Mouth disease, Multiple Fibrofolliculomas, Multiple Lipomata, Neoplasms, Oncocytoma of kidney, Oral submucous fibrosis, Oropharyngeal Dysphagia, Osteoporosis, Oxyphilic Adenoma, Papillary Renal Carcinoma, Papillary thyroid cancer, Parathyroid Adenoma, Parathyroid neoplasm, Patent foramen ovale, Pneumothorax, Polycystic kidney disease, Potocki-Lupski Syndrome, Pulmonary Emphysema, Receptive language delay, Renal Carcinoma, Renal cyst, Salivary gland oncocytoma, Sarcoma, Scoliosis, Skin disease, Skin Lesion, Skin neoplasm, Skin Neoplasms, Sleep Apnea, Smith-Magenis Syndrome, Spontaneous pneumothorax, Stereotyped Behavior, Stomach Carcinoma, Stomach Neoplasms, Thoracic disease, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm, Trichohepatoenteric Syndrome, Trigonocephaly, Tuberous Sclerosis, Tumor, Uveal melanoma, Von Hippel-Lindau Syndrome
|
917
|
|
|
Filaggrin |
ATOD2, FLG-1, FLG1 |
Curated: Asthma, Eczema, Ichthyosis vulgaris, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Contact dermatitis, Dermatitis, Atopic dermatitis, Ichthyosis, Insomnia, Respiratory system disease, Sebaceous gland disease, Skin disease
Unreviewed: Actinic keratosis, Agammaglobulinemia, X-Linked, Allergic rhinitis, Allergic Sensitization, Alopecia, Alopecia Areata, Alzheimer disease, Amyloidosis Cutis Dyschromia, Arthritis, Autism, Autoimmune Diseases, Avellino Corneal Dystrophy, Basal cell carcinoma, Bowen’s disease, Brain injuries, Breast Cancer, Breast neoplasm, Bronchiolitis, Burnett schwartz berberian syndrome, Carcinoma, Cerebellar Hypoplasia, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Cholangiocarcinoma, Chronic obstructive pulmonary disease, Colorectal neoplasm, Congenital Ichthyosis, Congenital Nonbullous Ichthyosiform Erythroderma, Contracture, Cutis marmorata, Dermatologic Disorders, Developmental Delay, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Dry eye syndrome, Dupuytren contracture, Dysmorphic Features, Dyssomnia, Eosinophilia, Epidermodysplasia Verruciformis, Epidermolysis Bullosa Pruriginosa, Gastroesophageal Reflux Disease, Glioma, Graft-Vs-Host Disease, Growth disorder, Heart disease, Hyperkeratosis, Epidermolytic, Hypersensitivity, Hypertension, Hypospadias, Ichthyosis Congenita, Ichthyosis Vulgaris, Impulse control disorder, Inflammatory Bowel Disease, Inflammatory Linear Verrucous Epidermal Nevus, Intellectual developmental disorder, Ischemic Stroke, Keratitis, Keratoconus, Keratosis pilaris, Leprosy, Lymphocytic Leukemia, Lymphoma, Malignant Neoplasm, Mammary Neoplasms, Melanoma, Metabolic syndrome, Microphthalmia with limb anomalies, Movement Disorders, Moyamoya Disease, Mucolipidosis, Myopia, Neoplasms, Netherton syndrome, Neuroblastoma, Nystagmus, Osteopenia, Pachyonychia Congenita, Pancreatic neoplasm, Placental Steroid Sulfatase Deficiency, Promyelocytic Leukemia, Pruritus, Psoriasis, Psoriasis vulgaris, Psoriatic Arthritis, Pulmonary arterial hypertension, Pulmonary hypertension, Respiratory Tract Diseases, Rheumatoid arthritis, Rhinitis, Sarcoidosis, Sarcoma, Schizophrenia, Skin Lesion, Skin neoplasm, Sleep Disorders, Spinocerebellar ataxia, Squamous cell carcinoma, Steroid Sulfatase Deficiency Disease, Stomach Carcinoma, Stomach neoplasms, Urticaria, Vitamin d deficiency
|
918
|
|
|
Filaggrin 2 |
IFPS, PSS6 |
Curated: Peeling skin syndrome, Systemic sclerosis
Unreviewed: Allergic contact dermatitis, Alzheimer disease, Amyloidosis Cutis Dyschromia, Atopic dermatitis, Avellino Corneal Dystrophy, Cognition disorder, Dermatitis, Dystonia, Eczema, Ichthyosis vulgaris, Lamellar ichthyosis, Ovarian neoplasm, Parakeratosis, Peeling Skin Syndrome, Pruritus, Sebaceous gland neoplasms, Sickle cell anemia
|
919
|
|
|
Fli-1 proto-oncogene, ETS transcription factor |
BDPLT21, EWSR2, FLI-1, SIC-1 |
Curated: Autoimmune thrombocytopenic purpura, Platelet-type bleeding disorder, Platelet disorder, Lymphocytic leukemia, Congenital left-sided heart lesions, Corneal astigmatism, Extraskeletal ewing sarcoma, Iga nephropathy, 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, Vitiligo, bleeding disorder, platelet-type, 21
Unreviewed: N/A
|
920
|
|
|
FOXP3 regulating long intergenic non-coding RNA |
- |
Curated: N/A
Unreviewed: N/A
|