Snyder-Robinson Syndrome

About the Disease
Intellectual Developmental Disorder, X-Linked, Syndromic, Snyder-Robinson Type, also known as mental retardation, x-linked, syndromic, snyder-robinson type, is related to syndromic x-linked intellectual disability snyder type and silver-russell syndrome 1, and has symptoms including seizures An important gene associated with Intellectual Developmental Disorder, X-Linked, Syndromic, Snyder-Robinson Type is SMS (Spermine Synthase). Affiliated tissues include bone, kidney and cortex, and related phenotypes are kyphoscoliosis and decreased muscle mass

Common Targets
SRM | CASR | SMS | NMDA receptor | NOS2 | ODC1

Note: If you'd like to get a target analysis report for Snyder-Robinson Syndrome, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Snyder-Robinson Syndrome at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

ACTH-independent Macronodular Adrenal Hyperplasia | Blood Protein Disorders | Hyperparathyroidism-jaw Tumor Syndrome | Varices | Gastroenteritis, Eosinophilic | VEXAS Syndrome | Sengers Syndrome | Multiple Sclerosis, Relapsing-remitting | Diabetes Type 2 | Blomstrand Osteochondrodysplasia | Cranial Nerve Disease | Choroiditis | Fibromyalgia | Gnathodiaphyseal Dysplasia | Neuroleptic Malignant Syndrome | Feingold Syndrome | Nephrotic Syndrome Type 1 | Imerslund-Grasbeck Syndrome | Intermittent Explosive Disorder | Ichthyosis | Chromosome 17q21.31 Deletion Syndrome | Dermatomyositis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Familial Retinal Arterial Macroaneurysm | Peeling Skin Syndrome Type B | Autosomal Recessive Congenital Ichthyosis | Myoclonic Epilepsy With Ragged Red Fibers | Hemorrhagic Disorders | Spinocerebellar Ataxia Type 1 | Partington Syndrome | PASLI Disease | Cholelithiasis | Pneumococcal Meningitis | Dystonia Musculorum Deformans | Epidermolytic Ichthyosis, Annular | Fibromuscular Dysplasia | Atelosteogenesis Type 2 | Duane Retraction Syndrome | Succinic Semialdehyde Dehydrogenase Deficiency | Congenital Diaphragmatic Hernia | Fuchs Dystrophy | Diffuse Mesangial Sclerosis | Poirier-Bienvenu Neurodevelopmental Syndrome | Hennekam Lymphangiectasia-lymphedema Syndrome | Spondylometaphyseal Dysplasia | Beta-Propeller Protein-associated Neurodegeneration | Relapsing Polychondritis | Spinocerebellar Ataxia Type 21 | Pierson Syndrome | Pulverulent Zonular Cataract | Aldosteronism | Trichorhinophalangeal Syndrome | Combined Deficiency Of Factor V And Factor VIII | Patent Foramen Ovale | Vogt-Koyanagi-Harada Syndrome | Addison Disease | Fibrosarcoma | Encephalitis, Tick-borne | Parkinson's Disease | Cri-du-chat Syndrome | Nicotine Addiction | Myocarditis | Ocular Surface Squamous Neoplasia | Aarskog-Scott Syndrome | Lattice Corneal Dystrophy | Hypertriglyceridemia | Kearns-Sayre Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Purpura | Waardenburg Syndrome Type 2E | Neovascular Glaucoma | Hermansky-Pudlak Syndrome | Scoliosis | Twin-to-twin Transfusion Syndrome | Interstitial Lung Diseases | Tuberculous Meningitis | Ornithine Transcarbamylase Deficiency | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Amebiasis | Silicosis | Lymphoproliferative Disorders | Gastric Atrophy | Precocious Puberty | Chronic Neutrophilic Leukemia | Pemphigus Foliaceus | Smoldering Myeloma | Intestinal Hypomagnesemia 1 | Fibrosis | Cryptococcal Meningitis | Spinocerebellar Ataxia Type 42 | Pseudoachondroplasia | Nail Disorder, Nonsyndromic Congenital | Apraxia | POEMS Syndrome | Carcinoma, Signet Ring Cell | Empyema | Infectious Diarrhea | Premature Ejaculation | Krabbe Disease | Hydronephrosis | Retinal Diseases | Polymyositis | Neuromuscular Disorders | Actinomycetoma | Hyperammonemia | Inflammatory Joint Disease | Inflammatory Myopathy | Mevalonate Kinase Deficiency | Pulmonary Capillary Hemangiomatosis | Pemphigus Vulgaris | Cerebrovascular Disorders | Primary Hyperoxaluria Type 3 | Becker Muscular Dystrophy | Best Macular Dystrophy | Diabetic Encephalopathy | Leiomyosarcoma | Achondrogenesis | Acral Lentiginous Melanoma | Epithelial-myoepithelial Carcinoma | Hypertrophy | CEDNIK Syndrome | Enhanced S-cone Syndrome | Dementia, Vascular | Barakat Syndrome | IMAGe Syndrome | Acromicric Dysplasia | ADNP Syndrome | Medulloblastoma | Leber Hereditary Optic Neuropathy | Aicardi-Goutieres Syndrome | Hereditary Spastic Paraplegia | Macular Degeneration | Metachromatic Leukodystrophy | Presbycusis | Transcobalamin Deficiency | Walker-Warburg Syndrome | Methemoglobinemia Type IV | Usher Syndrome Type I | Rosacea | Sporadic Inclusion Body Myositis | Neuronal Ceroid Lipofuscinosis | Speech Disorders | Craniolenticulosutural Dysplasia | Blastoma, Pleuropulmonary | CHARGE Syndrome | Opisthorchiasis | Cone Dystrophy | Obesity, Morbid | Charcot-Marie-Tooth Disease, Type 1A | Melanocytic Nevus | Craniopharyngioma | Lafora Disease | Cocaine-Related Disorders | Spinocerebellar Ataxia Type 7 | Hypodontia | Cockayne Syndrome | Hypotrichosis | Congenital Poikiloderma | Giant Cell Arteritis | Acute Kidney Injury | Congenital Aniridia | Liver Diseases | Schuurs-Hoeijmakers Syndrome | Thrombotic Microangiopathy | Congenital Central Hypoventilation Syndrome | Impulse Control Disorder | Acute Myeloid Leukemia | Esophageal Motility Disorders | Tay-Sachs Disease | Globozoospermia | Vitiligo | Anti-glomerular Basement Membrane Disease | Chronic Idiopathic Myelofibrosis | Hashimoto Thyroiditis | Congenital Stationary Night Blindness | Chronic Beryllium Disease | Progressive External Ophthalmoplegia | Encephalopathy, Ethylmalonic | Ovarian Sex Cord-stromal Tumor | Scapuloperoneal Spinal Muscular Atrophy | Rotor Syndrome | Wolman Disease | Richter's Syndrome | Cartilage Disorders | Heimler Syndrome | Hypotonia-cystinuria Syndrome | Fibrillation, Atrial | Left Ventricular Noncompaction | Smith-Magenis Syndrome | Steel Syndrome | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Retinitis Pigmentosa | Toxic Epidermal Necrolysis | Gardner Syndrome | Hyperostosis | Lymphomatoid Granulomatosis | Cryoglobulinemia | Eczema | Waldenstrom Macroglobulinemia | Familial Advanced Sleep Phase Syndrome | Vestibular Disease | Lissencephaly 2 | Venous Insufficiency | Exocrine Pancreatic Insufficiency | Stickler Syndrome | Meningitis | GATA2 Deficiency | Inflammatory Bowel Disease | Retinal Dystrophy | Microcephalic Primordial Dwarfism | Dermatofibrosarcoma | Farber Disease | Barrett Esophagus | Hypopituitarism | Stroke | Creatine Deficiency Syndrome | Primary Carnitine Deficiency | Fibrodysplasia Ossificans Progressiva | Preaxial Polydactyly | Amyotrophic Lateral Sclerosis | Cutaneous Mastocytosis | Parkinson Disease 6, Autosomal Recessive Early-onset | Alopecia Areata | Bietti Crystalline Dystrophy | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Episodic Ataxia | Congenital Ichthyosiform Erythroderma | Neurofibromatosis-Noonan Syndrome | Thymoma, Malignant | Postpartum Depression | Androgen Insensitivity | Osteogenesis Imperfecta Type IV | Kernicterus | Fragile X Syndrome | Alstrom Syndrome | Hyperparathyroidism, Secondary | Localized Scleroderma | Bloom Syndrome | Hypotrichosis Simplex | Shprintzen-Goldberg Syndrome | Phosphoglycerate Dehydrogenase Deficiency | Ghosal Syndrome | Polycystic Kidney, Autosomal Dominant | Granular Corneal Dystrophy | Bipolar Disorder | Congenital Nystagmus | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Zimmermann-Laband Syndrome | Cutaneous T-cell Lymphoma | Crimean-Congo Hemorrhagic Fever | Gerstmann-Straussler-Scheinker Syndrome | Glomerulonephritis, Membranoproliferative | Basal Ganglia Disease | Pyruvate Carboxylase Deficiency Disease | Spinocerebellar Ataxia Type 27 | Epithelioid Hemangioma | Tinea Versicolor | Adult Polyglucosan Body Disease | Congenital Afibrinogenemia | Malignant Peripheral Nerve Sheath Tumor | Waardenburg Syndrome Type 2 | Spinocerebellar Ataxia Type 12 | Thromboembolism | Sensory Neuropathy | Pneumothorax | Epilepsy, Generalized | CDKL5 Deficiency Disorder | Ehlers-Danlos Syndrome | Niemann-Pick Disease, Type B | Mucolipidosis Type III | Emery-Dreifuss Muscular Dystrophy | Hemoglobinopathies | Pendred Syndrome | Protein S Deficiency | Hemophilia | Sarcoidosis, Pulmonary | Glucagonoma | Omenn Syndrome | Antley-Bixler Syndrome | Prolymphocytic Leukemia | Spinocerebellar Ataxia Type 16 | Osteoporosis-pseudoglioma Syndrome | Neurofibrosarcoma | Malonyl-CoA Decarboxylase Deficiency | Alcoholism | Knobloch Syndrome | Scleritis | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Thyroid Dysgenesis | Pleurisy | Pseudohermaphroditism | Chondromyxoid Fibroma | Congenital Disorders Of Glycosylation Type II | Melanoma | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Epilepsy | Otosclerosis | Absence Epilepsy | Hepatitis C, Chronic | Autonomic Nervous System Disorders | Cardiac Arrest | Ectodermal Dysplasia | Neuroma | Blepharo-cheilo-odontic Syndrome | Thyroid Dyshormonogenesis | Hypotension, Orthostatic | Down Syndrome | Mucormycosis | 3-M Syndrome | Epidermolysis Bullosa Simplex With Mottled Pigmentation | McCune-Albright Syndrome | Bardet-Biedl Syndrome | Lupus Erythematosus | Congenital Bilateral Absence Of Vas Deferens | Polydactyly | Microcephaly | AIDS Dementia Complex | Liver Failure, Acute Infantile | Osmotic Demyelination Syndrome | Iron Deficiency Anemia | Pure Red Cell Aplasia | Non-Hodgkin Lymphoma | Shock, Cardiogenic | Microvillus Inclusion Disease | Werner's Syndrome | Pearson Syndrome | Myeloid Leukemia | MELAS Syndrome | Cat Eye Syndrome | Sialoadenitis | Lennox-Gastaut Syndrome | Familial Episodic Pain Syndrome | Aldosterone Synthase Deficiency | Juvenile Polyposis | Incontinentia Pigmenti | Congenital Hereditary Endothelial Dystrophy Type I | Congenital Sodium Diarrhea | Centronuclear Myopathy | Endometriosis | Cyclic Vomiting Syndrome | Depression | Chylomicron Retention Disease | Chylothorax, Congenital | Subacute Sclerosing Panencephalitis | Leukoplakia, Oral | Chorea-acanthocytosis | Metabolic Diseases | Neurocutaneous Syndromes | LRBA Deficiency | Paraplegia | Tyrosinemia Type 1 | X-linked Acrogigantism | Alpha-1 Antitrypsin Deficiency | KBG Syndrome | Idiopathic Pulmonary Fibrosis | Antenatal Bartter Syndrome Type 1 | Brooke-Spiegler Syndrome | Pseudomyxoma Peritonei | Ocular Hypertension | Cheilitis | Wagner Disease | Hartsfield Syndrome | Schizencephaly | Genitopatellar Syndrome | Fowler's Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Trichuriasis | Antisynthetase Syndrome | Prurigo Nodularis | Alagille Syndrome | Primary Erythromelalgia | Vertebrobasilar Insufficiency | Kleine-Levin Syndrome | Microphthalmia, Syndromic 7 | Gynecomastia | Meningococcal Infections | Coffin-Lowry Syndrome | Leber Congenital Amaurosis | Peutz-Jeghers Syndrome | Sarcoidosis | Pelizaeus-Merzbacher Disease | Heavy Chain Disease | Basal Ganglia Cerebrovascular Disease | Jawad Syndrome | X-linked Myotubular Myopathy | Diffuse Palmoplantar Keratoderma | Acrodermatitis | Congenital Stromal Corneal Dystrophy | Synpolydactyly | 3-methylglutaconic Aciduria Type IV | Coronary Heart Disease | Sleep Apnea | Nutrition Disorders | Anal Fissure | Cervicitis | Glomerulonephritis, Membranous | Alveolar Capillary Dysplasia | Polyomavirus Nephropathy | Crisponi Syndrome | Primary Torsion Dystonia