Disease

Silver-Russell Syndrome

About the Disease
Silver-Russell Syndrome 1, also known as silver-russell syndrome, is related to silver-russell syndrome due to 11p15 microduplication and silver-russell syndrome due to an imprinting defect of 11p15. An important gene associated with Silver-Russell Syndrome 1 is IGF2 (Insulin Like Growth Factor 2). The drugs Anastrozole and Aromatase Inhibitors have been mentioned in the context of this disorder. Affiliated tissues include eye, bone and brain, and related phenotypes are short stature and prominent forehead

Common Targets
KMT2C | NAP1L5 | MEG3 | GRB10 | MBTPS1 | ZMYND11 | TGM1 | SNU13 | PADI6 | PPIEL | NLRP5 | HMGA2 | GET1 | PLAG1 | G3480 | IGFBP1 | SNRPN | PLAGL1 | ZNF597 | GNAS-AS1 | ORC1 | ZFP42 | IGFBP3 | DLK1 | BSCL2 | BLM | RB1 | ANKRD11 | OSBPL5 | NNAT | FAM50B | KCNQ1OT1 | FGD1 | ZFP57 | SNURF | ZNF331 | NLRP2 | DIRAS3 | MCTS2 | SGCE | MEST | IGF2 | H19 | H19-ICR | CDKN1C | L3MBTL1 | TRIM37

疾病靶点研报
Silver-Russell Syndrome

Note: If you'd like to get a target analysis report for Silver-Russell 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 Silver-Russell Syndrome at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Alazami Syndrome | Progressive External Ophthalmoplegia | Pneumonia, Mycoplasma | Splenomegaly | Congenital Disorders Of Glycosylation Type II | Epidermolytic Ichthyosis, Annular | Seizures-scoliosis-macrocephaly Syndrome | Osteogenesis Imperfecta Type III | Autosomal Recessive Spastic Paraplegia Type 54 | Atopic Dermatitis | Autosomal Recessive Spastic Paraplegia Type 35 | Zellweger Syndrome | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Microcephaly, Seizures, And Developmental Delay | Anorchia | Autosomal Recessive Spastic Paraplegia Type 75 | Adult Polyglucosan Body Disease | Acrodermatitis Enteropathica | Postpoliomyelitis Syndrome | Kaposiform Hemangioendothelioma | Campomelic Dysplasia | Primary Hyperoxaluria Type 3 | Measles | DNA Ligase IV Deficiency | Epithelial-myoepithelial Carcinoma | Erythema Nodosum | Acquired Partial Lipodystrophy | Congenital Afibrinogenemia | Pleural Tuberculosis | Tremor | Pleomorphic Xanthoastrocytoma | Progressive Osseous Heteroplasia | Ocular Albinism Type 1 | Nephrotic Syndrome | Myelofibrosis | Tumoral Calcinosis | Ganglioglioma | Gangliosidosis | Skin Carcinoma | Malignant Peripheral Nerve Sheath Tumor | Progressive Familial Intrahepatic Cholestasis Type 2 | Hyperparathyroidism-jaw Tumor Syndrome | Acute Kidney Injury | Metatropic Dysplasia | Photosensitivity | Common Variable Immunodeficiency | Pulmonary Veno-occlusive Disease | Ichthyosis, X-linked | Angiosarcoma Of The Breast | Sleep Apnea | Carbonic Anhydrase VA Deficiency | Cancer, Prostate | Beare-Stevenson Syndrome | Chitayat Syndrome | Hypervalinemia | Hypercholesterolemia | Glutaric Aciduria Type 2 | Fukuyama Congenital Muscular Dystrophy | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Pulmonary Alveolar Proteinosis | Chronic Granulomatous Disease | Hemoglobinopathies | Gangliosidosis, GM1 | Multifocal Motor Neuropathy | Usher Syndrome Type II | Arterial Tortuosity Syndrome | Senior-Loken Syndrome | Pyloric Stenosis, Infantile Hypertrophic | Liebenberg Syndrome | Pseudohermaphroditism | Focal Cortical Dysplasia Type 2 | AIDS Dementia Complex | Pendred Syndrome | Basan Syndrome | Cherubism | Bernard-Soulier Syndrome | Opisthorchiasis | Cancer, Skin | Tuberculous Meningitis | Saul-Wilson Syndrome | Still Disease | Onchocerciasis | Iron Metabolism Disorders | Dyggve-Melchior-Clausen Disease | Raynaud Phenomenon | Presbyopia | Paroxysmal Nocturnal Hemoglobinuria | Hyperkeratosis | Mucolipidosis | Lymphedema-distichiasis Syndrome | Herpes Simplex Dermatitis | Diffuse Intrinsic Pontine Glioma | Osteonecrosis | Inflammatory Myofibroblastic Tumor | Pseudoachondroplasia | Sporadic Inclusion Body Myositis | B-cell Chronic Lymphocytic Leukemia | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Reflex Epilepsy | Hypercholesterolemia, Familial | Corneal Dystrophy | Congenital Tufting Enteropathy | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | GM2-gangliosidosis AB Variant | Vitiligo | Adrenoleukodystrophy, X-linked | Thyroiditis, Autoimmune | Veno-occlusive Disease | LRBA Deficiency | Phenylketonuria II | Basal Ganglia Cerebrovascular Disease | Polymicrogyria | Congenital Heart Block | PASLI Disease | Rhabdoid Tumor | Premenstrual Syndrome | Toxoplasmosis | Charcot-Marie-Tooth Disease, Type 2A | Majeed Syndrome | Melnick-Needles Syndrome | Apert Syndrome | Cataract | Epidermolytic Palmoplantar Keratoderma | Noonan Syndrome-like Disorder With Loose Anagen Hair | Kernicterus | Ellis-Van Creveld Syndrome | Pigment Dispersion Syndrome | Bronchitis, Chronic | Spondyloperipheral Dysplasia | Anemia | Optic Neuropathy | Achondrogenesis | N-acetylglutamate Synthase Deficiency | Macular Degeneration | Trismus-pseudocamptodactyly Syndrome | Blau Syndrome | Micropenis | Leukemia | Polyomavirus Nephropathy | Autism Spectrum Disorders | Large Granular Lymphocytic Leukemia | Myoclonic Epilepsy With Ragged Red Fibers | Pilomatrix Carcinoma | Glycogen Storage Disease | Vasculitis | Viral Meningitis | Renal Medullary Carcinoma | Familial Retinal Arterial Macroaneurysm | Lymphoma, Follicular | Spondylocarpotarsal Synostosis Syndrome | Aneurysm, Thoracic Aortic | Oligoasthenoteratozoospermia | Mitochondrial Disease | Hyperparathyroidism | GATA2 Deficiency | Spinocerebellar Ataxia Type 27 | Chronic Idiopathic Myelofibrosis | Spinocerebellar Ataxia Type 10 | Mucormycosis | Cannabis Abuse | Batten Disease | Synpolydactyly | Spinocerebellar Ataxia Type 2 | Pseudohypoparathyroidism Type 1B | Creatine Deficiency Syndrome Due To AGAT Deficiency | Blomstrand Osteochondrodysplasia | Spondylometaphyseal Dysplasia | Thalassemia | Shprintzen-Goldberg Syndrome | Coronary Artery Disease | Multiple Myeloma | Sjogren Syndrome | Esthesioneuroblastoma | Meesmann Corneal Dystrophy | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Central Retinal Artery Occlusion | Cerebellofaciodental Syndrome | Diabetes Type 1 | Superficial Spreading Melanoma | Epicondylitis | Otopalatodigital Syndrome Type 2 | Lymphedema | Myositis | Danon Disease | Aplasia Cutis Congenita | Spinocerebellar Ataxia Type 3 | Ataxia-ocular Apraxia 2 | Cyst | Basal Ganglia Disease, Biotin-responsive | Vitreoretinopathy, Proliferative | Patent Ductus Arteriosus | Familial Hemiplegic Migraine | Hemangioendothelioma | Celiac Disease | Oculocutaneous Albinism Type 4 | Urticaria | Arthrogryposis | Corneal Dystrophies, Hereditary | Malnutrition | Hyperostosis | Aceruloplasminemia | Hoyeraal-Hreidarsson Syndrome | Hypospadias | Lymphomatoid Granulomatosis | Asplenia | Leigh Syndrome | Hypersomnia | Hypopigmentation | Liver Diseases | Pachyonychia Congenita | Jaundice, Obstructive | PHARC Syndrome | Jalili Syndrome | Brenner Tumor | Barrett Esophagus | Cushing Syndrome | Thyroiditis | Schwannoma | Long QT Syndrome Type 3 | Tyrosinemia | Chronic Kidney Disease | Chordoma | Colitis, Lymphocytic | Gingivitis | Porokeratosis | X-linked Charcot-Marie-Tooth Disease | Neurocutaneous Syndromes | Incontinentia Pigmenti | Pancreatitis | Cerebral Amyloid Angiopathy | Adenoid Cystic Carcinoma | Giant Cell Arteritis | Usher Syndrome Type III | Cutis Laxa | Cholecystitis | Stuve-Wiedemann Syndrome | Hyperferritinemia-cataract Syndrome | Charcot-Marie-Tooth Disease Type 2E | Pierson Syndrome | Migraine | Bietti Crystalline Dystrophy | Lyme Disease | Chorea | Central Pain Syndrome | Insulin Resistance | KBG Syndrome | Hereditary Spastic Paraplegia | Thanatophoric Dysplasia | Myoclonic Atonic Epilepsy | Gerstmann-Straussler-Scheinker Syndrome | Hyperinsulinemic Hypoglycemia | Acute Coronary Syndrome | Uveitis, Anterior | Hypertensive Nephropathy | Infertility, Male | Dominant Optic Atrophy | Malaria, Cerebral | Purpura, Thrombotic Thrombocytopenic | Gyrate Atrophy Of The Choroid And Retina | Alpers Syndrome | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Malaria | Dystonia Musculorum Deformans | Marfan Syndrome | Hereditary Inclusion Body Myopathy | Peutz-Jeghers Syndrome | Hypodontia | Krabbe Disease | Hemophagocytic Lymphohistiocytosis | Pelvic Inflammatory Disease | Acute Chest Syndrome | Kabuki Syndrome 2 | Lentigo | Schnyder Crystalline Corneal Dystrophy | Hydrocephalus | Hyperlipidemia Type V | Pseudohypoparathyroidism Type 1A | Sarcoidosis | Schizophrenia, Paranoid | Sarcoma, Endometrial Stromal | Bronchiolitis | Leukoplakia, Oral | Blue Rubber Bleb Nevus Syndrome | Tricho-hepato-enteric Syndrome | Dengue Hemorrhagic Fever | Urofacial Syndrome | Spinocerebellar Ataxia Type 23 | Citrullinemia | Congenital Nystagmus | Angiosarcoma | Xeroderma Pigmentosum Variant Type | Gastroenteritis | Nicolaides-Baraitser Syndrome | Acute Generalized Exanthematous Pustulosis | Metachondromatosis | Intermittent Explosive Disorder | Pain | Sezary Syndrome | Exotropia | Chudley-McCullough Syndrome | Milk Allergy | Erythema Multiforme | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Jawad Syndrome | Lymphoma Lymphoblastic | Exfoliative Dermatitis | Primary Carnitine Deficiency | Osteosclerosis | Pelizaeus-Merzbacher Disease | Hepatitis B, Chronic | Intermittent Claudication | Progressive Familial Intrahepatic Cholestasis | Babesiosis | Demyelinating Diseases | Aldosterone Synthase Deficiency | Lesch-Nyhan Syndrome | Headache | Multiple Sulfatase Deficiency | Hereditary Mixed Polyposis Syndrome | Cabezas Syndrome | Hereditary Pyropoikilocytosis | Ichthyosis Hystrix, Curth-Macklin Type | Galactosemia | Hyperammonemia | Takayasu's Arteritis | Epilepsy, Generalized | Pterygium | Facioscapulohumeral Muscular Dystrophy Type 1 | Interstitial Lung Diseases | Thyroid Dyshormonogenesis | Postaxial Polydactyly | Pyruvate Decarboxylase Deficiency | Cryptosporidiosis | CDKL5 Deficiency Disorder | Neurofibroma | Benign Familial Infantile Seizures | Trichomegaly | FG Syndrome | Gestational Trophoblastic Disease | Peripheral Neuropathy | Pineoblastoma | Wagner Disease | Varices | Pregnancy, Ectopic | Craniolenticulosutural Dysplasia | Polymyalgia Rheumatica | Olmsted Syndrome | Homocystinuria | Keratoconjunctivitis | Brachydactyly | Oligodendroglioma | Lipoma | Peeling Skin Syndrome Type B | Hyperbilirubinemia | Histoplasmosis | Diabetic Neuropathy | Fascioliasis | Sensorineural Hearing Loss | Intestinal Obstruction | Hyperthermia, Malignant | Carbohydrate Metabolism Disorders | ICF Syndrome | Frontometaphyseal Dysplasia | Hypoglycemia | Arthritis, Gouty | Learning Disability | Peritonitis | Oligoastrocytoma | Tendinitis | Gitelman Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Spasticity | Kindler Syndrome | Fanconi Anemia | Lichen Planus | Agammaglobulinemia | Leishmaniasis, Cutaneous | Pure Autonomic Failure | Thrombotic Microangiopathy | Keratocystic Odontogenic Tumor | Apraxia | Juvenile Hyaline Fibromatosis | NGLY1 Deficiency | Inflammatory Bowel Disease | Chromosome 9q34.3 Deletion Syndrome | Temporal Lobe Epilepsy | Autonomic Neuropathy | Amenorrhea | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Meningitis | Apparent Mineralocorticoid Excess Syndrome | Chronic Granulomatous Disease, X-linked | Situs Inversus | Congenital Diaphragmatic Hernia | Barakat Syndrome | Infertility | Periventricular Nodular Heterotopia | Hydrocephalus, Normal Pressure | Methemoglobinemia | Protein C Deficiency