Disease

Neurofibroma

About the Disease
Neurofibroma, also known as neurofibromas, is related to epithelioid neurofibroma and pacinian tumor, and has symptoms including back pain, headache and pain. An important gene associated with Neurofibroma is NF1 (Neurofibromin 1), and among its related pathways/superpathways are Disease and ERK Signaling. The drugs Methylphenidate and Dopamine have been mentioned in the context of this disorder. Affiliated tissues include skin, trachea and breast, and related phenotypes are plexiform neurofibroma and periarticular subcutaneous nodules

Common Targets
TAGLN | G4233 | G2064 | NF1 | RASSF1 | G673 | G7157

疾病靶点研报
Neurofibroma

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

Other Diseases

Rosacea | Inflammatory Linear Verrucous Epidermal Nevus | Epidermolysis Bullosa Dystrophica | Microcephaly, Seizures, And Developmental Delay | Lafora Disease | Osteitis | Hyperthermia, Malignant | Ophthalmia, Sympathetic | Fuchs Dystrophy | Endocarditis | Usher Syndrome | Diabetic Nephropathy | Clouston Hidrotic Ectodermal Dysplasia | Nephrotic Syndrome Type 1 | Double Outlet Right Ventricle | Acne | Pontocerebellar Hypoplasia | Sick Sinus Syndrome | Adams-Oliver Syndrome | Lymphoma, Mantle Cell | Lattice Corneal Dystrophy | Thrombophlebitis | Mandibuloacral Dysplasia With Type A Lipodystrophy | Phosphoglycerate Dehydrogenase Deficiency | Prediabetes | Plasma Cell Dyscrasia | Neurodegeneration With Brain Iron Accumulation | Rhabdomyosarcoma, Embryonal | Scleroderma | Tendinitis | Mevalonate Kinase Deficiency | Silicosis | Schistosomiasis | Desbuquois Syndrome | Fucosidosis | Coloboma | Atherosclerosis | Spondyloepiphyseal Dysplasia Tarda, X-linked | Autosomal Recessive Spastic Paraplegia Type 35 | Leukocyte Adhesion Deficiency Type 1 | Borderline Personality Disorder | Nemaline Myopathy 8 | Axenfeld-Rieger Syndrome | Vitiligo | Thrombosis | Alopecia Totalis | Stickler Syndrome | Familial Hemiplegic Migraine | Rickets | Hyperferritinemia-cataract Syndrome | Skin Carcinoma | Micro Syndrome | Encephalocele | Mitochondrial DNA Depletion Syndrome | Cholangitis | Niemann-Pick Disease, Type C | Metabolic Diseases | Pseudo-pseudohypoparathyroidism | Epidermolytic Ichthyosis, Annular | Cardiac Sarcoidosis | Craniopharyngioma | Chromosome 8q21.11 Deletion Syndrome | Spinal And Bulbar Muscular Atrophy | Primary Carnitine Deficiency | Macrodactyly | Myopia | Lymphoproliferative Disease, X-linked | POEMS Syndrome | Benign Recurrent Intrahepatic Cholestasis 1 | Binge Eating Disorder | Hemophagocytic Lymphohistiocytosis | Nasodigitoacoustic Syndrome | Bethlem Myopathy | Primary Cutaneous Amyloidosis | Sjogren Syndrome | Bladder Exstrophy | Osteogenesis Imperfecta Type III | Cholestasis | Hepatic Veno-occlusive Disease | Williams Syndrome | Dent Disease | Hyperandrogenemia | Wolman Disease | Trichomegaly | Oligodendroglioma | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Hemolytic Anemia | Diarrhea | Gray Platelet Syndrome | Fontaine Progeroid Syndrome | Congenital Fiber-type Disproportion Myopathy | Multiple Epiphyseal Dysplasia | Polycystic Ovary Syndrome | Peroxisomal Disorder | Carcinoma, Merkel Cell | Snyder-Robinson Syndrome | Glycogen Storage Disease Type 1 | Branchiootorenal Syndrome | Orotic Aciduria | Obesity | Harlequin Ichthyosis | Ophthalmoplegia | Uveitis | Acute Lymphocytic Leukemia | Premature Ejaculation | Huntington's Disease-like 2 | Polycythemia Vera | Spinocerebellar Ataxia Type 20 | Blepharophimosis Syndrome | Facioscapulohumeral Muscular Dystrophy | Seborrheic Dermatitis | Hyperkeratosis | Brooke-Spiegler Syndrome | Acute Tubular Necrosis | Brachydactyly | Osteochondrosis | Retinoschisis | Oculocutaneous Albinism Type 1 | Overactive Bladder | Bipolar Disorder | Spinal Muscular Atrophy Type 2 | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Light Chain Amyloidosis | Heterotaxy | Dysfibrinogenemia | Low Tension Glaucoma | Spondylolisthesis | Pityriasis Rubra Pilaris | Hyperacusis | Spinocerebellar Ataxia Type 31 | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Follicular Dendritic Cell Sarcoma | Leri-Weill Dyschondrosteosis | Cystinosis | Congenital Primary Aphakia | Hemoglobinopathies | Vaginitis | Neuroectodermal Tumors, Primitive | Epidermolytic Palmoplantar Keratoderma | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Hepatitis, Chronic | Hydrocephalus, Normal Pressure | Renal Medullary Carcinoma | Patent Ductus Arteriosus | Osteosarcoma | Vitreoretinopathy, Proliferative | Hypertension, Renovascular | Bardet-Biedl Syndrome | Becker Muscular Dystrophy | Chronic Inflammatory Demyelinating Polyneuropathy | Congenital Hemolytic Anemia | Intermittent Claudication | Chromosome 9q34.3 Deletion Syndrome | Scleritis | Cone Dystrophy | Campomelic Dysplasia | Non-epidermolytic Palmoplantar Keratoderma | Usher Syndrome Type II | Melanocytic Nevus | Osmotic Demyelination Syndrome | Otopalatodigital Syndrome Type 2 | Cancer, Kidney | Dyggve-Melchior-Clausen Disease | Spinocerebellar Ataxia Type 17 | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Colitis | Metachondromatosis | Combined Deficiency Of Factor V And Factor VIII | Rolandic Epilepsy | Panuveitis | Macular Corneal Dystrophy Type 1 | Coenzyme Q10 Deficiency | Chronic Enteropathy Associated With SLCO2A1 Gene | Malonyl-CoA Decarboxylase Deficiency | Neuronal Ceroid Lipofuscinosis | Epidermolysis Bullosa Simplex, Generalized | Familial Hypobetalipoproteinemia | Pierson Syndrome | Fanconi Anemia | Trichothiodystrophy | Alopecia Areata | Thromboembolism | Amebiasis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Costello Syndrome | Adenoma, Pleomorphic | Congenital Sodium Diarrhea | Endometriosis | Vascular Cognitive Impairment | DICER1 Syndrome | Metabolic Syndrome | Autoimmune Hemolytic Anemia | Congenital Bile Acid Synthesis Defect | Liddle Syndrome | Oligospermia | Glutaric Aciduria Type 2 | Rotor Syndrome | Hyperkalemic Periodic Paralysis | Cardiomyopathy, Dilated, 1L | Benign Familial Infantile Seizures | Cerebellar Ataxia, Cayman Type | Learning Disability | Renal Dysplasia | Hypothalamic Obesity | Microphthalmia | Primary Progressive Nonfluent Aphasia | Citrullinemia | Alzheimer Disease, Late Onset | Acral Lentiginous Melanoma | Choroideremia | Gnathodiaphyseal Dysplasia | Pleurisy | Infantile Spasm | Cystinuria | Turner's Syndrome | Hypoalbuminemia | Neurogenic Bladder | Loeys-Dietz Syndrome Type 4 | Impetigo | Transient Bullous Dermolysis Of The Newborn | Iron Overload | Isovaleric Acidemia | Stiff-man Syndrome | Gaucher Disease | GNE Myopathy | Arrhythmogenic Right Ventricular Cardiomyopathy | Chordoma | Chondromyxoid Fibroma | Alpha-1 Antitrypsin Deficiency | Hemangioma | Scoliosis | Epithelioid Hemangioma | Usher Syndrome Type I | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | LMNA-related Congenital Muscular Dystrophy | Hemophilia | Hepatopulmonary Syndrome | Spondyloperipheral Dysplasia | Argininosuccinic Aciduria | Trimethylaminuria | Uremia | Blastoma, Pleuropulmonary | Meningeal Melanocytoma | Chondrodysplasia Punctata | Oligoasthenoteratozoospermia | Lactose Intolerance | Polycythemia | Antiphospholipid Syndrome | Choroiditis | Primary Lateral Sclerosis | Periventricular Nodular Heterotopia | Agoraphobia | Uterine Leiomyoma | Mitochondrial Cytopathy | Tenosynovial Giant Cell Tumor | Glycogen Storage Disease | Seizures-scoliosis-macrocephaly Syndrome | Plasmacytoma | Congestive Heart Failure | Asthma, Exercise-induced | AIDS Dementia Complex | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Peutz-Jeghers Syndrome | Retinitis Pigmentosa 3 | Leishmaniasis, Cutaneous | Okihiro Syndrome | X-linked Acrogigantism | Gerodermia Osteodysplastica | Diabetes | Cervicitis | Echinococcosis | Ligneous Conjunctivitis | Dengue Shock Syndrome | Optic Atrophy 2 | Hereditary Elliptocytosis | Extramammary Paget's Disease | Blepharospasm | Cenani-Lenz Syndactyly Syndrome | Muir-Torre Syndrome | Hereditary Spherocytosis | Hereditary Neuropathy With Liability To Pressure Palsies | Diabetes Insipidus, Nephrogenic | Congenital Absence Of Vas Deferens | Proctitis | Hepatitis D | Dental Caries | Chronic Neutrophilic Leukemia | Kawasaki Disease | Noonan Syndrome-like Disorder With Loose Anagen Hair | Avellino Corneal Dystrophy | LEOPARD Syndrome | Babesiosis | Corneal Ulcer | Asperger Syndrome | Pneumonia, Viral | Leukemia-lymphoma, Adult T-cell | Renal Tubular Dysgenesis | Dystrophy, Cone-rod | Smoldering Myeloma | Thin Basement Membrane Disease | Triphalangeal Thumb-polysyndactyly Syndrome | Cardiomyopathy, Hypertrophic | WAGR Syndrome | Measles | Hypercalcemia | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Toxoplasmosis | Werner's Syndrome | Retinal Detachment | Imerslund-Grasbeck Syndrome | Gallstones | Esophageal Carcinoma | HUPRA Syndrome | Celiac Disease | Intermittent Explosive Disorder | Osteomalacia | Klippel-Feil Syndrome | Kidney Stones | Chanarin-Dorfman Syndrome | Epicondylitis | Optic Neuropathy | Congenital Central Hypoventilation Syndrome | Hyperinsulinemic Hypoglycemia | Acute Anterior Uveitis | Pelvic Inflammatory Disease | Pseudohypoparathyroidism Type 2 | Blood Protein Disorders | Fuchs Heterochromic Iridocyclitis | Keratocystic Odontogenic Tumor | Congenital Generalized Lipodystrophy | Alazami Syndrome | Familial Dysautonomia | Hemochromatosis Type 1 | Osteosclerosis | Acromicric Dysplasia | Paraganglioma, Carotid Body | Leigh Syndrome | Myotonia | Moyamoya Disease | Colon Adenoma | Porokeratosis | Heart Failure | Photosensitivity | Hypopigmentation | Glycogen Storage Disease Type 9 | Interstitial Lung Diseases | Progressive Familial Intrahepatic Cholestasis Type 3 | Esophagitis | Temtamy Preaxial Brachydactyly Syndrome | Sarcoma, Endometrial Stromal | Cole-Carpenter Syndrome | Hepatitis | Dysplastic Nevus | Frontometaphyseal Dysplasia | Dementia | Rett Syndrome | Retinal Vasculitis | Primary Hyperoxaluria | Erythema Nodosum | Large Granular Lymphocytic Leukemia | Primary Familial Brain Calcification | Iron Metabolism Disorders | Pemphigus Foliaceus | Schistosomiasis Mansoni | Cannabis Abuse | Meningioma | Schizoaffective Disorder | Familial Hyperaldosteronism | Autism | Adrenal Insufficiency | Paroxysmal Nocturnal Hemoglobinuria | Mucormycosis | Mast Cell Leukemia | Hypogammaglobulinemia | Amyotrophic Lateral Sclerosis, Juvenile | Nijmegen Breakage Syndrome | Metanephric Adenoma | Cohen Syndrome | Familial Exudative Vitreoretinopathy | Familial Mediterranean Fever | Poirier-Bienvenu Neurodevelopmental Syndrome | Lymphoma, Follicular | Stromal Corneal Dystrophy | Hyperinsulinemia | Chordoid Glioma | Polymyositis | Wiedemann-Steiner Syndrome | Congenital Stromal Corneal Dystrophy | Coffin-Siris Syndrome | Tylosis With Esophageal Cancer | Neuroma | Glutaric Aciduria Type 3 | Spinocerebellar Ataxia Type 42 | Crouzon Syndrome With Acanthosis Nigricans | Anorchia | Hemorrhagic Disorders | Atelosteogenesis Type 1 | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Oligoastrocytoma | Restrictive Dermopathy