Disease

Schwannomatosis

About the Disease
Neurilemmomatosis, also known as schwannomatosis, is related to schwannomatosis 1 and neurofibromatosis, type i. An important gene associated with Neurilemmomatosis is SMARCB1 (SWI/SNF Related, Matrix Associated, Actin Dependent Regulator Of Chromatin, Subfamily B, Member 1), and among its related pathways/superpathways are Assembly of the pre-replicative complex and Chromatin organization. The drugs Tanezumab and Mitogens have been mentioned in the context of this disorder. Affiliated tissues include skin, small intestine and spinal cord, and related phenotypes are Increased Nanog expression and Increased Nanog expression

Common Targets
LZTR1 | G1029 | DGCR8 | SMARCA4

疾病靶点研报
Schwannomatosis

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

Other Diseases

Pierre Robin Syndrome | Retinoblastoma | Autosomal Recessive Spastic Paraplegia Type 54 | Diabetes Insipidus, Neurogenic | Polycystic Ovary Syndrome | Microcephaly, Seizures, And Developmental Delay | Epithelial-myoepithelial Carcinoma | Charcot-Marie-Tooth Disease Type 2E | Huntington's Disease | Schistosomiasis Mansoni | Polyneuropathy | Adult Polyglucosan Body Disease | Hereditary Elliptocytosis | Oculocutaneous Albinism Type 1 | Schistosomiasis | Spinocerebellar Ataxia Type 10 | Nephroblastoma | Multiple Myeloma | Bethlem Myopathy | Sarcoma, Endometrial Stromal | Neutropenia | Nance-Horan Syndrome | Blepharophimosis Syndrome | Meesmann Corneal Dystrophy | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Menetrier Disease | Multiple Epiphyseal Dysplasia | Primary Cutaneous Amyloidosis | Infantile Refsum Disease | Nemaline Myopathy 10 | Familial Male-limited Precocious Puberty | Muir-Torre Syndrome | Melanocytic Nevus | Seminoma | Oligospermia | Amelanotic Melanoma | Kallmann Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Hyperlipidemia, Familial Combined | Heterotaxy | Corneal Neovascularization | Polydactyly | Anorexia Nervosa | Peroxisomal Disorder | Corneal Dystrophies, Hereditary | Ichthyosis | Adrenal Insufficiency | Methemoglobinemia | Hyperlipidemia | Lymphedema-distichiasis Syndrome | Eclampsia | Conjunctivitis, Allergic | Lipid Storage Diseases | Hyperphenylalaninemia | Barrett Esophagus | Myopathy | Endocarditis | WAGR Syndrome | Schwartz-Jampel-Aberfeld Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Polyarteritis Nodosa | IgA Deficiency | Chronic Neutrophilic Leukemia | Hyperinsulinism-hyperammonemia Syndrome | Conjunctivitis | Hydrocephalus | Acrodermatitis | Schnyder Crystalline Corneal Dystrophy | Incontinentia Pigmenti | 3-methylglutaconic Aciduria | Cutaneous Lupus Erythematosus | Calcium Pyrophosphate Deposition Disease | Dystonia-parkinsonism, X-linked | Takayasu's Arteritis | Lymphoma Lymphoblastic | Congenital Adrenal Hyperplasia 1 | Periventricular Leukomalacia | Schamberg Disease | Juvenile Polyposis | Stuttering | Chromosome 9q34.3 Deletion Syndrome | Osteosclerosis | Anemia | Inflammatory Myopathy | Sitosterolemia | Pernicious Anemia | Autosomal Recessive Spastic Paraplegia Type 35 | Porphyria, Variegate | Chorioretinitis | Hyperhomocysteinemia | Irritable Bowel Syndrome | Myelomeningocele | Saul-Wilson Syndrome | Porphyria Cutanea Tarda | HELLP Syndrome | Craniofrontonasal Syndrome | Chronic Lymphocytic Leukemia | Tatton-Brown-Rahman Syndrome | Leprosy | Biotinidase Deficiency | Fetal Akinesia Deformation Sequence | Common Cold | Pachyonychia Congenita | Dystonia | Inborn Errors Of Metabolism | Spinocerebellar Ataxia Type 12 | Hyperuricemia | Lipodystrophy | Aspartylglycosaminuria | Stromal Corneal Dystrophy | Congenital Nystagmus | Hartnup Disease | Eczema | Malignant Peripheral Nerve Sheath Tumor | Pseudo-pseudohypoparathyroidism | Ganglioglioma | Lassa Fever | Bartter Syndrome | Coronary Restenosis | Cystitis, Interstitial | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Hyper IgE Syndrome | Chromosome 5q Deletion Syndrome | Otitis Media | Melanoma, Uveal | Temtamy Preaxial Brachydactyly Syndrome | Nager Acrofacial Dysostosis | Familial Mediterranean Fever | Raine Syndrome | Myoclonic Atonic Epilepsy | Lactose Intolerance | X-linked Sideroblastic Anemia | 3-M Syndrome | Alpha-mannosidosis | Methylmalonic Acidemia | Long QT Syndrome Type 1 | Adenoma, Pleomorphic | Vici Syndrome | Hemangioma | Osteogenesis Imperfecta Type VI | Acrodysostosis | Bicuspid Aortic Valve | Astrocytoma, Anaplastic | VACTERL Association | Periodic Limb Movement Disorder | Specific Granule Deficiency | Polycystic Kidney, Autosomal Recessive | Arrhythmogenic Right Ventricular Cardiomyopathy | Diabetes Type 2 | Intellectual Disability, Autosomal Dominant 5 | Hepatitis C, Chronic | Delayed Sleep Phase Syndrome | Esophageal Carcinoma | Carpenter Syndrome | Osteogenesis Imperfecta Type I | Parkinsonism | Prurigo Nodularis | Hydronephrosis | Graves Disease | Dominant Optic Atrophy | Familial Thoracic Aortic Aneurysm | Myelitis, Transverse | Medulloblastoma | Hyperoxaluria | Amyotrophic Lateral Sclerosis, Juvenile | Oculocutaneous Albinism Type 2 | Alzheimer Disease, Late Onset | Alcoholism | Congenital Hypofibrinogenemia | Epidermolysis Bullosa | Gastroenteritis, Eosinophilic | Autoimmune Disease | Erysipelas | Diverticulitis | Gardner Syndrome | Infantile Neuroaxonal Dystrophy | Periodontitis | Persistent Truncus Arteriosus | Tyrosinemia Type 1 | Hypercholesterolemia, Familial | Osteitis | Hypodontia | Syphilis | Transcobalamin Deficiency | Necrotizing Autoimmune Myopathy | Niemann-Pick Disease | Hypotension, Orthostatic | Spinocerebellar Ataxia Type 7 | Cheilitis | Duane Retraction Syndrome | Hyperparathyroidism, Primary | Pathological Gambling | Connective Tissue Disorders | Acromegaly | Blastoma, Pleuropulmonary | Epilepsy | Anterior Segment Dysgenesis | Nijmegen Breakage Syndrome | Sotos Syndrome | Arterial Tortuosity Syndrome | Hemangioblastoma | Vestibular Disease | Warsaw Breakage Syndrome | Aldosterone Synthase Deficiency | Primary Biliary Cholangitis | Behavioral Variant Of Frontotemporal Dementia | Mitochondrial Cytopathy | Geleophysic Dysplasia | X-linked Acrogigantism | Pyloric Stenosis, Infantile Hypertrophic | Personality Disorders | Oculocutaneous Albinism Type 4 | Immunoproliferative Disorders | Renal Medullary Carcinoma | Charcot-Marie-Tooth Disease Type 4D | Thyroiditis, Autoimmune | Fibrillation, Atrial | Usher Syndrome Type III | Endometritis | Stroke, Hemorrhagic | Contact Dermatitis | Diastrophic Dysplasia | Obesity | Congenital Ichthyosiform Erythroderma | Richter's Syndrome | Central Pain Syndrome | Intracranial Hypertension | Dementia | Diffuse Mesangial Sclerosis | Charcot-Marie-Tooth Disease, Type 2C | Carbonic Anhydrase VA Deficiency | Cancer, Bladder | Melnick-Needles Syndrome | Delirium | 3-methylglutaconic Aciduria Type IV | Thalassemia | Insulin Resistance | Carcinoma, Signet Ring Cell | Hodgkin Lymphoma | Depression | Desbuquois Syndrome | Neuroleptic Malignant Syndrome | Multifocal Motor Neuropathy | Spinal Muscular Atrophy Type 3 | Central Core Disease | Learning Disability | Paraganglioma | Keratitis-ichthyosis-deafness Syndrome | Cerebral Cavernous Malformations | Syncope | KBG Syndrome | Milk Allergy | Hoyeraal-Hreidarsson Syndrome | Thromboembolism | Carey-Fineman-Ziter Syndrome | Cockayne Syndrome | Diabetic Macular Edema | Behcet's Disease | Bardet-Biedl Syndrome | Parkinson's Disease | Hemimegalencephaly | Joubert Syndrome 2 | Sarcoma | Lymphangioma | Epidermolytic Palmoplantar Keratoderma | Chediak-Higashi Syndrome | Hereditary Pyropoikilocytosis | Hereditary Xerocytosis | Carcinoma, Small Cell | Hemosiderosis | Cranial Nerve Disease | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Carbamoyl Phosphate Synthetase I Deficiency | Atrial Septal Defect | Leukoencephalopathy, Progressive Multifocal | Coffin-Siris Syndrome | Pneumothorax | Bronchiolitis | Thrombocythemia, Essential | Mucolipidosis Type III | Hypothyroidism | Cholecystitis | Shwachman-Bodian-Diamond Syndrome | Polymyositis | X-linked Charcot-Marie-Tooth Disease | Thanatophoric Dysplasia | Angelman Syndrome | Sclerocornea | Rheumatoid Arthritis | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Episodic Ataxia Type 2 | Glycogen Storage Disease Type 5 | Osteogenesis Imperfecta Type V | Chondromyxoid Fibroma | Renal-hepatic-pancreatic Dysplasia | Small Lymphocytic Lymphoma | Infertility, Male | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Spinocerebellar Ataxia Type 16 | Asphyxia Neonatorum | Dystonia Musculorum Deformans | Distal Spinal Muscular Atrophy | Wolff-Parkinson-White Syndrome | Lipoma | Lewy Body Dementia | Guillain-Barre Syndrome | Pre-eclampsia | Pigment Dispersion Syndrome | Esophagitis, Eosinophilic | Hyperuricemic Nephropathy, Familial Juvenile | Aldosteronism | Sporadic Hemiplegic Migraine | Avellino Corneal Dystrophy | Histiocytic Sarcoma | Zollinger-Ellison Syndrome | Loeys-Dietz Syndrome | Cysticercosis | Neurocutaneous Syndromes | Sjogren Syndrome | Chordoma | Xeroderma Pigmentosum | Leri Pleonosteosis | Nail Disorder, Nonsyndromic Congenital | Carney Triad | Pulmonary Stenosis | Cyst | Odonto-onycho-dermal Dysplasia | POEMS Syndrome | Dwarfism | Dysgerminoma | Phenylketonuria | Creutzfeldt-Jakob Disease | Intermittent Explosive Disorder | Focal Segmental Glomerulosclerosis | Atelosteogenesis Type 2 | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Cervicitis | Cataract | Vitelliform Macular Dystrophy | Amyotrophic Lateral Sclerosis | Autoimmune Autonomic Ganglionopathy | Ganglioneuroma | 3C Syndrome | Infectious Diarrhea | Thin Basement Membrane Disease | Mitochondrial DNA Depletion Syndrome 13 | Osteomyelitis | Disseminated Superficial Actinic Porokeratosis | GNE Myopathy | Congenital Disorders Of Glycosylation Type II | Rett Syndrome | Overactive Bladder | Goiter, Nodular | Split Hand-foot Malformation | Norrie Disease | Idiopathic Multicentric Castleman Disease | Lennox-Gastaut Syndrome | Tetraplegia | Restrictive Dermopathy | Presbycusis | Creatine Deficiency Syndrome | Hypohidrotic Ectodermal Dysplasia | Ocular Hypertension | Colitis, Collagenous | Bronchitis | Spinocerebellar Ataxia Type 6 | Congenital Generalized Lipodystrophy | Cryptosporidiosis | Genee-Wiedemann Syndrome | Mevalonate Kinase Deficiency | Pyruvate Carboxylase Deficiency Disease | Pouchitis | Miyoshi Myopathy | Retinal Diseases | Pituitary Disorders | Colorectal Adenoma | Stroke | Endometriosis | Osteogenesis Imperfecta Type IV | Chudley-McCullough Syndrome | Hemorrhagic Disorders | Thrombosis | Multicentric Carpotarsal Osteolysis Syndrome | Epithelioid Hemangioma | Alstrom Syndrome | Impetigo | Pneumococcal Meningitis | Hernia, Inguinal | Werner's Syndrome | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Arteriovenous Malformations | Hashimoto Thyroiditis | Peyronie's Disease | Wilson's Disease | Best Macular Dystrophy | Glanzmann Thrombasthenia | Anuria | Motion Sickness | Optic Neuropathy | Melanoma