Sertoli Cell-only Syndrome
Sertoli Cell-only Syndrome
About the Disease
Spermatogenic Failure, X-Linked, 1, also known as sertoli cell-only syndrome, is related to testicular cancer and testicular disease. An important gene associated with Spermatogenic Failure, X-Linked, 1 is CFAP47 (Cilia And Flagella Associated Protein 47), and among its related pathways/superpathways is Male infertility. Affiliated tissues include Testis, testes and pituitary, and related phenotypes are obesity and gynecomastia
Common Targets
DMRT1 | FSHR | HELQ | DICER1 | G367 | FSHB

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Other Diseases
Rhabdomyosarcoma, Embryonal | Benign Recurrent Intrahepatic Cholestasis 1 | Myasthenia | Persistent Fetal Circulation | Thrombocytopenia | Hemorrhoids | Schnyder Crystalline Corneal Dystrophy | Progressive Familial Intrahepatic Cholestasis Type 1 | Retinal Vasculitis | Sepiapterin Reductase Deficiency | Feingold Syndrome | Basal Ganglia Disease | Hypospadias | Amebiasis | Dermatomyositis | Aicardi-Goutieres Syndrome | Fuchs Dystrophy | Pfeiffer Syndrome | Tietze Syndrome | Porokeratosis | Borderline Personality Disorder | Cantu Syndrome | Amyotrophic Lateral Sclerosis | Leukemia-lymphoma, Adult T-cell | Toxoplasmosis | Potocki-Shaffer Syndrome | Acute Leukemia | Neuromyelitis Optica | Benign Familial Infantile Seizures | Hereditary Neuropathy With Liability To Pressure Palsies | Autoimmune Hemolytic Anemia | Retinal Dystrophy | Pancreatitis, Chronic | Muscular Dystrophy | Neovascular Glaucoma | Charcot-Marie-Tooth Disease Axonal Type 2N | Antithrombin III Deficiency | Congenital Stromal Corneal Dystrophy | Loeys-Dietz Syndrome Type 4 | Hypersomnia | Epidermolysis Bullosa | Pyelonephritis | Onchocerciasis | Chondromyxoid Fibroma | Gangliosidosis | Dysthymia | Adams-Oliver Syndrome | Epithelial-myoepithelial Carcinoma | Guttate Psoriasis | Ectopia Lentis, Isolated, Autosomal Recessive | Budd-Chiari Syndrome | Myelitis | Renal Hypouricemia | Contact Dermatitis | Saethre-Chotzen Syndrome | Diffuse Intrinsic Pontine Glioma | Connective Tissue Disorders | Peeling Skin Syndrome, Acral Type | Autosomal Recessive Spastic Paraplegia Type 35 | Sick Sinus Syndrome 1 | Cardiomyopathy, Restrictive | Aarskog-Scott Syndrome | Spasticity | Neuronal Ceroid Lipofuscinosis | Lymphoproliferative Disease, X-linked | Dysplastic Nevus | Persistent Mullerian Duct Syndrome | Nicotine Addiction | Bursitis | Thrombasthenia | Polymicrogyria | Cervical Dystonia | Sickle Cell Disease | Venous Insufficiency | Ovarian Hyperstimulation Syndrome | Dental Caries | Malonyl-CoA Decarboxylase Deficiency | Overactive Bladder | Hydrocephalus | Spondylolisthesis | Cerebral Cavernous Malformations | Glycogen Storage Disease Type 1a | Pontocerebellar Hypoplasia Type 7 | Trichuriasis | 5-oxoprolinase Deficiency | Zollinger-Ellison Syndrome | Sarcoidosis | Familial Dysautonomia | Alkaptonuria | Osteoarthritis | Hypereosinophilic Syndrome | Deafness, Dystonia, And Cerebral Hypomyelination | Congenital Absence Of Vas Deferens | Aneurysm, Thoracic Aortic | Tic Disorder | Patent Ductus Arteriosus | Auriculocondylar Syndrome | Tangier Disease | Acanthosis Nigricans | Hemochromatosis Type 1 | Gangliosidosis, GM1 | VEXAS Syndrome | Inflammatory Myofibroblastic Tumor | Heimler Syndrome | FG Syndrome | Leukoplakia, Oral | Myoclonic Epilepsy With Ragged Red Fibers | Anorectal Malformations | Donnai-Barrow Syndrome | Parapsoriasis | Spinal Muscular Atrophy | Exfoliative Dermatitis | Nanophthalmos | Hypercholesterolemia | Spinocerebellar Ataxia Type 31 | Empyema | Neurocutaneous Syndromes | 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Defects | Hypersensitivity | Diverticulitis | Zellweger Syndrome | Metachromatic Leukodystrophy | Progressive Familial Intrahepatic Cholestasis Type 3 | Homocystinuria | Aspergillosis | Peroxisomal Disorder | Postpartum Depression | Birt-Hogg-Dube Syndrome | Hodgkin Lymphoma | Tendinopathy | Thalassemia, Beta | Plasmacytoma | Cholangiocarcinoma | Hereditary Sensory And Autonomic Neuropathy | Ligneous Conjunctivitis | Pontocerebellar Hypoplasia | Hepatoblastoma | Congenital Generalized Lipodystrophy | Jacobsen Syndrome | Adult Polyglucosan Body Disease | Hepatic Adenomatosis | Goldenhar Syndrome | Alcoholism | Essential Fructosuria | Hyperparathyroidism, Secondary | Hidradenitis | Porphyria | Anodontia | Cerebral Amyloid Angiopathy | Aspartylglycosaminuria | Polycystic Kidney, Autosomal Recessive | Hypermethioninemia | Schwartz-Jampel-Aberfeld Syndrome | Malnutrition | Mandibuloacral Dysplasia With Type A Lipodystrophy | Trichorhinophalangeal Syndrome | Congenital Muscular Dystrophy | Okihiro Syndrome | VACTERL Association | Keratoconjunctivitis | Arrhythmogenic Right Ventricular Cardiomyopathy | Long QT Syndrome Type 3 | Panuveitis | Lassa Fever | Proopiomelanocortin Deficiency | Lafora Disease | Postaxial Polydactyly | Cardiomyopathy, Peripartum | Wiskott-Aldrich Syndrome | Glioblastoma | Congenital Ichthyosiform Erythroderma | Alstrom Syndrome | Transthyretin-related Amyloidosis | Primary Biliary Cholangitis | Robinow Syndrome | Hemimegalencephaly | Hereditary Coproporphyria | Adenoma, Villous | Peripheral T-cell Lymphoma | Vestibular Disease | Metanephric Adenoma | Ichthyosis, X-linked | CDKL5 Deficiency Disorder | Protein S Deficiency | Sporadic Hemiplegic Migraine | Alopecia Totalis | Lymphedema-distichiasis Syndrome | Impulse Control Disorder | Vitamin K Deficiency | Corneal Edema | Pendred Syndrome | Pantothenate Kinase-associated Neurodegeneration | Holt-Oram Syndrome | Ventricular Septal Defect | Martsolf Syndrome | Eiken Syndrome | Adenomyosis | Cancer, 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Microphthalmia | Larsen Syndrome | Harlequin Ichthyosis | Frontotemporal Dementia | Niemann-Pick Disease | Pelvic Inflammatory Disease | Granular Corneal Dystrophy Type 1 | Tendinitis | Asthma | Kawasaki Disease | Obesity, Morbid | Alopecia Areata | Citrullinemia | Polycystic Kidney, Autosomal Dominant | Asthma, Nocturnal | Renal Oncocytoma | Fibrosis | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Anencephaly | Arthritis, Gouty | Saul-Wilson Syndrome | Myelomeningocele | C3 Glomerulopathy | Nephrotic Syndrome Type 1 | Sponastrime Dysplasia | Hereditary Spastic Paraplegia | Gallstones | Stiff-man Syndrome | Spinocerebellar Ataxia Type 23 | Gyrate Atrophy Of The Choroid And Retina | Basal Ganglia Disease, Biotin-responsive | Focal Facial Dermal Dysplasia | Posterior Polar Cataract | Dystonia Musculorum Deformans | Inborn Errors Of Metabolism | Diabetes Mellitus, Transient Neonatal | Imerslund-Grasbeck Syndrome | Fascioliasis | Congenital Poikiloderma | Pitt-Hopkins Syndrome | Pleurisy | Spinocerebellar Ataxia Type 2 | Antiphospholipid Syndrome | Acne | Cold Agglutinin Disease | CEDNIK Syndrome | Osmotic Demyelination Syndrome | Common Variable Immunodeficiency | Joubert Syndrome 2 | Cutaneous T-cell Lymphoma | Macrophagic Myofasciitis | Gastroenteritis, Eosinophilic | Hyper IgE Syndrome | Multiple Sclerosis, Chronic Progressive | Congenital Torticollis | Camptocormia | Hennekam Lymphangiectasia-lymphedema Syndrome | Schuurs-Hoeijmakers Syndrome | Noonan Syndrome | Panniculitis | Hyperthermia, Malignant | Glycogen Storage Disease Type 0 | Familial Hypertrophic Cardiomyopathy | Pituitary Stalk Interruption Syndrome | Polyarteritis Nodosa | Purpura, Thrombotic Thrombocytopenic | Olmsted Syndrome | Chanarin-Dorfman Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Gingivitis | Distal Myopathy | Multiple Hamartoma Syndrome | Scleroderma, Diffuse | Dysfibrinogenemia | Thrombophilia | Smith-Kingsmore Syndrome | Myofibrillar Myopathy | Hepatitis B, Chronic | Medulloblastoma | Nager Acrofacial Dysostosis | Congenital Central Hypoventilation Syndrome | 3C Syndrome | Dyskeratosis Congenita | Anal Fissure | Behcet's Disease | Vitiligo | Rhinitis | Syndactyly | Albinism | Diffuse Palmoplantar Keratoderma | Pancytopenia | Angiosarcoma | Seborrheic Dermatitis | Charcot-Marie-Tooth Disease Type 3 | Cancer, Colon | Enhanced S-cone Syndrome | Hernia, Inguinal | Peyronie's Disease | Spondylocarpotarsal Synostosis Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Spinocerebellar Ataxia Type 5 | Cocaine-Related Disorders | Angioedema, Acquired | Melanoma | Charcot-Marie-Tooth Disease Type 2T | Acrodermatitis Enteropathica | Pemphigus | Melnick-Needles Syndrome | Lymphoma, AIDS-related | Perry Syndrome | Neurotoxicity | Addison Disease | Charcot-Marie-Tooth Disease Type 4B1 | Intestinal Obstruction | Encephalocele | Varices | Congenital Myasthenic Syndrome | Multiple System Atrophy | Hereditary Folate Malabsorption | Keratocystic Odontogenic Tumor | Epithelioid Hemangioma | Photosensitivity | Pineoblastoma | Cataplexy | Glycogen Storage Disease Type 1 | Binge Eating Disorder | Agoraphobia | Hyperlipidemia Type V | Mucormycosis | Hereditary Pyropoikilocytosis | Li-Fraumeni Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Wolfram Syndrome 2 | Lipid Storage Myopathy | Osteogenesis Imperfecta