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

Vitreoretinal Degeneration, Snowflake Type | Juvenile Myoclonic Epilepsy | Myelitis | Anal Fissure | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Sertoli Cell-only Syndrome | Tetanus | Alpha-thalassemia Myelodysplasia Syndrome | Chediak-Higashi Syndrome | Cutaneous Angiosarcoma | Hemophilia | Hyperparathyroidism-jaw Tumor Syndrome | Cryptorchidism | Pseudoachondroplasia | Ovarian Hyperstimulation Syndrome | Sponastrime Dysplasia | Pituitary Dwarfism | Hamartoma | Atherosclerosis | Autosomal Recessive Spastic Paraplegia Type 75 | Keratoconjunctivitis | Epilepsy | Celiac Disease | Malnutrition | Cirrhosis | Lymphangioleiomyomatosis | Cholestasis, Intrahepatic | Chronic Thromboembolic Pulmonary Hypertension | Renal-hepatic-pancreatic Dysplasia | Paracoccidioidomycosis | Absence Epilepsy | Nephronophthisis | Schistosomiasis | Melanoma, Malignant | Urolithiasis | Pneumonia, Viral | Osteochondrosis | Hypothalamic Obesity | Whipple's Disease | Bulimia Nervosa | Irritable Bowel Syndrome | Hyperferritinemia-cataract Syndrome | Hypertension, Renal | Mucolipidosis | Leukemia | Varicocele | Waardenburg Syndrome Type 4 | Persistent Fetal Circulation | Seasonal Mood Disorder | Spinocerebellar Ataxia Type 10 | Acute Lymphocytic Leukemia | Familial Partial Lipodystrophy | X-linked Creatine Transporter Deficiency | Pneumoconiosis | Pseudohypoparathyroidism Type 2 | Congenital Hereditary Endothelial Dystrophy Type I | Avian Influenza | Pathological Gambling | Neurocysticercosis | Weill-Marchesani Syndrome | Oligodendroglioma | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Diabetic Neuropathy | Cataract | Tumoral Calcinosis | Gigantism | Goldenhar Syndrome | Phosphoglycerate Dehydrogenase Deficiency | Tuberculous Meningitis | Myelitis, Transverse | Chronic Periodontitis | Botulism | Congenital Sodium Diarrhea | Tardive Dyskinesia | Gerstmann-Straussler-Scheinker Syndrome | Familial Male-limited Precocious Puberty | Peritonitis | Lentigo | MIRAGE Syndrome | Dwarfism | Endophthalmitis | Vitamin A Deficiency | Tonsillitis | Primary Familial Brain Calcification | Monilethrix | Sengers Syndrome | Cluster Headache | Carcinoma, Small Cell | Fanconi Syndrome | Relapsing Polychondritis | PHARC Syndrome | Carey-Fineman-Ziter Syndrome | Pantothenate Kinase-associated Neurodegeneration | Gaucher Disease | Acute Kidney Injury | Amyloidosis | Xeroderma Pigmentosum | Nutrition Disorders | Diabetic Encephalopathy | Cardiomyopathy, Restrictive | Canavan Disease | Prune Belly Syndrome | Schizotypal Personality Disorder | Kindler Syndrome | Lymphomatoid Granulomatosis | Pupil Disorders | Keratosis, Actinic | Guillain-Barre Syndrome | Basal Ganglia Disease, Biotin-responsive | Chronic Granulomatous Disease | Renal Dysplasia | Pulmonary Vein Stenosis | Cystitis | Iron Deficiency Anemia | CDKL5 Deficiency Disorder | Otitis Media | Autosomal Recessive Spastic Paraplegia Type 35 | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Retinopathy, Diabetic | Cholangitis | Cholesteryl Ester Storage Disease | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Von Willebrand Disease | Diarrhea | Barrett Esophagus | Angiodysplasia | Hashimoto Thyroiditis | Rift Valley Fever | LEOPARD Syndrome | Nanophthalmos | B-cell Prolymphocytic Leukemia | Osteoporosis | Congenital Disorders Of Glycosylation Type II | Fragile X Syndrome | DiGeorge Syndrome | Persistent Truncus Arteriosus | Angiomyolipoma | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Polymyalgia Rheumatica | Progressive Myoclonic Epilepsy | Myoclonus-dystonia Syndrome | Abetalipoproteinemia | Antisocial Personality Disorder | Charcot-Marie-Tooth Disease, Type 2C | Aspergillosis | Papilloma | Lichen Sclerosus | Exostoses | Multiple Sclerosis | Microtia | Marshall-Smith Syndrome | Waardenburg Syndrome Type 4A | Carotid Artery Disease | Epidermolytic Palmoplantar Keratoderma | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Pycnodysostosis | Anemia | Thyroid Dysgenesis | Enhanced S-cone Syndrome | Netherton Syndrome | Neuromuscular Disorders | Persistent Mullerian Duct Syndrome | Mitochondrial Myopathy | Pulmonary Stenosis | Hemimegalencephaly | Pain | Early Infantile Epileptic Encephalopathy 28 | Dementia | Ganglioglioma | Obesity, Morbid | Hyperkeratosis | Hypospadias | Jacobsen Syndrome | Kearns-Sayre Syndrome | Osteogenesis Imperfecta | Gardner Syndrome | Insulinoma | Uveitis, Anterior | Myopathy | Heimler Syndrome | Intermittent Claudication | Charcot-Marie-Tooth Disease Type 3 | Leber Hereditary Optic Neuropathy | Myopia | Osteomyelitis | Steel Syndrome | Thrombocytopenia | Keratoacanthoma | Tuberculosis | Multiple Sulfatase Deficiency | Cabezas Syndrome | Jawad Syndrome | Carcinoid Syndrome | Oral Lichen Planus | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Sporadic Hemiplegic Migraine | Spinal Cord Diseases | Pleomorphic Xanthoastrocytoma | Conn Syndrome | Epidermolytic Hyperkeratosis | Chromosome 9q34.3 Deletion Syndrome | Craniosynostosis | Zellweger Syndrome | Pemphigoid | Essential Fructosuria | Charcot-Marie-Tooth Disease, Type 2 | Nemaline Myopathy | Pemphigus Foliaceus | Spondylometaphyseal Dysplasia | Retinal Detachment | Megaloblastic Anemia | Graft-versus-host Disease | Acrodermatitis Enteropathica | Pleurisy | Amyotrophic Lateral Sclerosis, Juvenile | Dentinogenesis Imperfecta | Spinocerebellar Ataxia Type 27 | Marfan Syndrome | Duane Retraction Syndrome | Eclampsia | Pneumonia, Mycoplasma | Vitamin B12 Deficiency | Hyper IgE Syndrome | Citrullinemia | Ghosal Syndrome | Hydronephrosis | Mevalonate Kinase Deficiency | Hepatopulmonary Syndrome | Iron Overload | Orotic Aciduria | Dyskeratosis Congenita | Blepharo-cheilo-odontic Syndrome | Meningeal Melanocytoma | Trachoma | Usher Syndrome Type I | Cerebral Amyloid Angiopathy | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Systemic Mastocytosis | Encephalitis | Ventricular Septal Defect | Spinal And Bulbar Muscular Atrophy | Hyperphenylalaninemia | Hypertension, Pulmonary | Lactose Intolerance | Hereditary Coproporphyria | X-linked Sideroblastic Anemia | Hemosiderosis | Proctitis | Bicuspid Aortic Valve | Skin Carcinoma | Cryoglobulinemia | Long QT Syndrome Type 2 | Granular Corneal Dystrophy Type 1 | Leukoplakia | Primary Ovarian Insufficiency | Autosomal Recessive Congenital Ichthyosis | Agnathia-Otocephaly Complex | Thyroiditis | Woodhouse-Sakati Syndrome | Chronic Kidney Disease | Burn-McKeown Syndrome | Acute Chest Syndrome | Oculocutaneous Albinism Type 1 | Hidradenitis Suppurativa | Exotropia | Porphyria, Variegate | Learning Disability | WAGR Syndrome | Methylmalonic Acidemia | Cardiac Arrest | Cancer, Prostate | Hypertensive Retinopathy | Trimethylaminuria | Keratitis-ichthyosis-deafness Syndrome | Huntington's Disease | Chronic Leukemia | TARP Syndrome | Emery-Dreifuss Muscular Dystrophy | Carcinoma, Transitional Cell | Uremia | Brugada Syndrome 1 | Familial Isolated Hyperparathyroidism | Intestinal Pseudo-obstruction | Stevens-Johnson Syndrome | Plasma Cell Dyscrasia | Infectious Diarrhea | Cystinosis | Thyroid Hormone Resistance | Cenani-Lenz Syndactyly Syndrome | Retinal Dystrophy | Craniometaphyseal Dysplasia | Panniculitis | Osmotic Demyelination Syndrome | Gastric Atrophy | Sick Sinus Syndrome | Kallmann Syndrome | Primary Hyperoxaluria Type 1 | Spondylosis | Angiosarcoma Of The Breast | Beta-Propeller Protein-associated Neurodegeneration | Greenberg Dysplasia | Fetal Akinesia Deformation Sequence | Familial Hemiplegic Migraine | IgA Deficiency | Carbonic Anhydrase VA Deficiency | Fontaine Progeroid Syndrome | Conjunctivitis, Allergic | Azoospermia | Acromicric Dysplasia | Creutzfeldt-Jakob Disease | Schnyder Crystalline Corneal Dystrophy | Colitis, Lymphocytic | Arterial Tortuosity Syndrome | Hemangioendothelioma | Precocious Puberty | Dyslipidemia | Melanoma, Uveal | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Melnick-Needles Syndrome | Transthyretin-related Amyloidosis | Paroxysmal Kinesigenic Dyskinesia | Sarcoidosis, Pulmonary | Alcoholism | Shprintzen-Goldberg Syndrome | Bartsocas-Papas Syndrome | Acanthosis Nigricans | Synovitis | Pyruvate Dehydrogenase Deficiency | Hypoplastic Left Heart Syndrome | Urethritis | Diverticulitis | Hyperbilirubinemia, Neonatal | Conduct Disorder | Fahr Disease | GM2-gangliosidosis AB Variant | Dermatitis | Goiter | Phenylketonuria II | Borjeson-Forssman-Lehmann Syndrome | Mandibuloacral Dysplasia With Type A Lipodystrophy | 3-methylcrotonyl-CoA Carboxylase Deficiency | Cholera | Hepatic Adenomatosis | Dominant Optic Atrophy | CHOPS Syndrome | Familial Digital Arthropathy-brachydactyly | Pulmonary Alveolar Proteinosis | Photosensitivity | Chorioretinitis | Acral Lentiginous Melanoma | Ichthyosis, X-linked | Paraplegia | Polycythemia | Lipodystrophy | Presbyopia | Glaucomatocyclitic Crisis | Measles | Axenfeld-Rieger Syndrome | Beare-Stevenson Syndrome | Dental Caries | Short-chain Acyl-CoA Dehydrogenase Deficiency | Arrhythmogenic Right Ventricular Cardiomyopathy | Blepharospasm | Kaposiform Hemangioendothelioma | Supravalvular Aortic Stenosis | Lysosomal Acid Lipase Deficiency | Familial Mediterranean Fever | Chronic Lymphocytic Leukemia | Restless Legs Syndrome | Retinoschisis | Malonyl-CoA Decarboxylase Deficiency | Arts Syndrome | Aplasia Cutis Congenita | SAPHO Syndrome | Sarcosinemia | Liebenberg Syndrome | Cutaneous Lupus Erythematosus | X-linked Myotubular Myopathy | Progressive Familial Intrahepatic Cholestasis Type 1 | Communication Disorders | Sporadic Inclusion Body Myositis | Saethre-Chotzen Syndrome | Rotor Syndrome | Raynaud Phenomenon | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Vestibular Disease | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Plasmacytoma | Pterygium | Spinocerebellar Ataxia Type 14 | Hypolipoproteinemia | Stuttering | Hypertension | Hypogammaglobulinemia | Leukoplakia, Oral | Myelofibrosis | Megalencephaly | Familial Advanced Sleep Phase Syndrome | Neovascular Glaucoma | Bernard-Soulier Syndrome