Myofibromatosis

About the Disease
Infantile Myofibromatosis, also known as lipofibromatosis, is related to lipofibromatosis-like neural tumor and myofibroma. An important gene associated with Infantile Myofibromatosis is PDGFRB (Platelet Derived Growth Factor Receptor Beta), and among its related pathways/superpathways are ERK Signaling and Signal Transduction. The drug Cola has been mentioned in the context of this disorder. Affiliated tissues include skin, pancreas and lung, and related phenotypes are subcutaneous nodule and neoplasm of the skin

Common Targets
PDGFRB

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

Other Diseases

Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Tyrosinemia Type 2 | Multifocal Motor Neuropathy | Hypogonadism | Sialidosis | Hoyeraal-Hreidarsson Syndrome | Chronic Leukemia | Creatine Deficiency Syndrome Due To AGAT Deficiency | Craniolenticulosutural Dysplasia | Birk-Barel Syndrome | Multiple System Atrophy | Neuroectodermal Tumors, Primitive | Hypertrophy | Acanthosis Nigricans | Teratozoospermia | Adenomatoid Tumor | Congenital Diaphragmatic Hernia | T-cell Lymphoma, Subcutaneous Panniculitis-like | Progressive Familial Intrahepatic Cholestasis Type 3 | Retinal Dystrophy | Cholera | Uremia | Pyelonephritis | Esthesioneuroblastoma | Pyruvate Kinase Deficiency | Moyamoya Disease | Blastoma, Pleuropulmonary | Connective Tissue Disorders | Osteoporosis-pseudoglioma Syndrome | Rolandic Epilepsy | Duodenal Atresia | Psoriasis | Mastitis | Autoimmune Autonomic Ganglionopathy | Hepatitis A | Hypothyroidism | Pierson Syndrome | Antenatal Bartter Syndrome Type 1 | Carcinoma, Transitional Cell | Succinic Semialdehyde Dehydrogenase Deficiency | Pseudohermaphroditism | Hereditary Spastic Paraplegia | Localized Scleroderma | Epithelial-myoepithelial Carcinoma | Ovarian Sex Cord-stromal Tumor | Hypertension, Essential | Pouchitis | Congenital Stationary Night Blindness | Asplenia | Achondrogenesis | Kaposiform Hemangioendothelioma | Restrictive Dermopathy | PHARC Syndrome | Ocular Albinism Type 1 | Megalencephaly | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Eosinophilic Asthma | Crisponi Syndrome | Renal Oncocytoma | Leukodystrophies | Familial Advanced Sleep Phase Syndrome | Fascioliasis | Jawad Syndrome | Cryopyrin-associated Periodic Syndromes | Methemoglobinemia Type IV | Meniere's Disease | Alveolar Capillary Dysplasia | Nephrotic Syndrome Type 1 | Granular Corneal Dystrophy | Hereditary Neuropathy With Liability To Pressure Palsies | Charcot-Marie-Tooth Disease, Type 6 | Pemphigus | Isovaleric Acidemia | Myoclonic Atonic Epilepsy | Silicosis | Stroke, Hemorrhagic | Bladder Exstrophy | Hepatitis, Alcoholic | Benign Familial Infantile Seizures | Hypopituitarism | Non-Hodgkin Lymphoma | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Basan Syndrome | Tetanus | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Erythema Nodosum | Rheumatoid Arthritis | Fatty Aldehyde Dehydrogenase Deficiency | Cellulitis | Cancer, Colon | Hypertension, Renovascular | Basal Cell Nevus Syndrome | Hemorrhoids | Anovulation | Ichthyosis Hystrix, Curth-Macklin Type | Hyperparathyroidism, Primary | Glycogen Storage Disease Type 5 | Genee-Wiedemann Syndrome | Nephrotic Syndrome | Acute Kidney Injury | Short-chain Acyl-CoA Dehydrogenase Deficiency | Hypertension, Portal | Hyperammonemia | Infectious Diarrhea | Methemoglobinemia | Greig Cephalopolysyndactyly Syndrome | Osteosclerosis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Okihiro Syndrome | Pontocerebellar Hypoplasia Type 7 | Synovitis | Cystinosis | Diabetic Encephalopathy | Schnyder Crystalline Corneal Dystrophy | Krabbe Disease | Delayed Sleep Phase Syndrome | MELAS Syndrome | Motor Neuron Diseases | Cleidocranial Dysplasia | T-cell Prolymphocytic Leukemia | Primary Progressive Nonfluent Aphasia | Non-bullous Congenital Ichthyosiform Erythroderma | Neuromuscular Disorders | Hepatitis B, Chronic | Pancreatitis | Cerebral Cavernous Malformations | Cardiomyopathy, Restrictive | Tibial Muscular Dystrophy | Plasma Cell Dyscrasia | Paraganglioma | Rickets | Glanzmann Thrombasthenia | Creatine Deficiency Syndrome | Cardiomyopathy, Peripartum | Neuropathy | Vestibular Disease | Pontocerebellar Hypoplasia Type 2 | Intestinal Pseudo-obstruction | Toxoplasmosis | Smith-Magenis Syndrome | Hepatitis C, Chronic | Osteonecrosis Of The Jaw | Pseudohypoparathyroidism Type 2 | Spondylocarpotarsal Synostosis Syndrome | Acute Leukemia | Large Granular Lymphocytic Leukemia | Nestor-Guillermo Progeria Syndrome | Barrett Esophagus | Autoimmune Hemolytic Anemia | Vascular Cognitive Impairment | Stuve-Wiedemann Syndrome | Cerebellofaciodental Syndrome | Persistent Fetal Circulation | Choroideremia | Hypolipoproteinemia | Cirrhosis | Iron Deficiency Anemia | Shock, Cardiogenic | Peutz-Jeghers Syndrome | Wilson's Disease | Charcot-Marie-Tooth Disease Type 4D | Vitamin B12 Deficiency | Vasculitis | Nephritis, Interstitial | Skin Carcinoma | Aspartylglycosaminuria | Melanoma, Malignant | Chondrodysplasia Punctata 1, X-linked Recessive | Osteochondrosis | Presbyopia | Stromal Corneal Dystrophy | Kernicterus | Gallstones | Protein S Deficiency | Cancer, Lung | Lichen Sclerosus | Lipodystrophy | AIDS Dementia Complex | Hemimegalencephaly | Neurodermatitis | Erythromelalgia | Yellow Fever | Glycogen Storage Disease Type 9 | Hydrocephalus | Muscle Wasting | Spinal Muscular Atrophy | Macrophagic Myofasciitis | Early Infantile Epileptic Encephalopathy | IgA Nephropathy | Atrial Septal Defect | Microcephalic Primordial Dwarfism | Optic Neuropathy, Anterior Ischemic | Congenital Fiber-type Disproportion Myopathy | Osteogenesis Imperfecta Type V | Adenocarcinoma | Occipital Neuralgia | Dentinogenesis Imperfecta | Autosomal Recessive Bestrophinopathy | Dyslipidemia | Pneumococcal Meningitis | Kleine-Levin Syndrome | Glycogen Storage Disease Type 1a | Chronic Kidney Disease | Blepharoconjunctivitis | Familial Digital Arthropathy-brachydactyly | Myelomeningocele | Pontocerebellar Hypoplasia | Fibrosis | Panic Disorder | Benign Hereditary Chorea | Subacute Sclerosing Panencephalitis | Saethre-Chotzen Syndrome | Leukemia-lymphoma, Adult T-cell | Primary Erythromelalgia | Dent Disease | Pilomatrix Carcinoma | Addison Disease | Angioedema | N-acetylglutamate Synthase Deficiency | Primary Lateral Sclerosis | Ophthalmia, Sympathetic | Cole-Carpenter Syndrome | CDKL5 Deficiency Disorder | Prolactinoma | Anal Fissure | Twin-to-twin Transfusion Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Ichthyosis, X-linked | Necrobiosis Lipoidica | Hypoproteinemia, Hypercatabolic | Gnathodiaphyseal Dysplasia | Acute Chest Syndrome | Toxic Epidermal Necrolysis | Tuberculosis | Sialidosis Type I | Progressive Familial Intrahepatic Cholestasis Type 2 | Charcot-Marie-Tooth Disease Axonal Type 2N | Cri-du-chat Syndrome | X-linked Sideroblastic Anemia | AIDS | Loeys-Dietz Syndrome Type 4 | Auriculocondylar Syndrome | Familial Isolated Hyperparathyroidism | Hypermethioninemia | Palsy, Cerebral | Angioimmunoblastic T-cell Lymphoma | Familial Pheochromocytoma-paraganglioma | Johanson-Blizzard Syndrome | Uveitis, Anterior | Ghosal Syndrome | Chylomicron Retention Disease | Heroin Dependence | Riboflavin Transporter Deficiency Neuronopathy | C3 Glomerulonephritis | Analgesia | Sponastrime Dysplasia | Idiopathic Pulmonary Fibrosis | Roberts Syndrome | Retinal Detachment | Hypertensive Retinopathy | Rubinstein-Taybi Syndrome | Dental Caries | Papilledema | Cholecystitis | Xeroderma Pigmentosum Variant Type | Amyotrophic Lateral Sclerosis | Renal Failure | Glioma | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Glycogen Storage Disease Type 3 | Renal Dysplasia | Hereditary Sensory And Autonomic Neuropathy | Joubert Syndrome 2 | Peroxisomal Disorder | Larsen Syndrome | CEDNIK Syndrome | Lipoma | Sengers Syndrome | Congenital Aniridia | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Monilethrix | Intestinal Tuberculosis | Asthma, Exercise-induced | Multiple Epiphyseal Dysplasia | Bernard-Soulier Syndrome | Ophthalmoplegia | Leri Pleonosteosis | Craniometaphyseal Dysplasia | Vascular Calcification | Keratopathy | Diabetes Insipidus | Exocrine Pancreatic Insufficiency | Rhabdomyosarcoma | Gardner Syndrome | Crigler-Najjar Syndrome | Primary Progressive Aphasia | Erysipelas | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Periventricular Nodular Heterotopia | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Communication Disorders | Adenoma, Pleomorphic | Cholestasis | Sensory Neuropathy | Placenta Previa | Dupuytren Disease | Endometriosis | Juvenile Polyposis | Familial Cerebral Amyloid Angiopathy | Otitis Media | Metabolic Syndrome | Homocystinuria | Asthma | Pseudoexfoliation Syndrome | Spastic Paraplegia Type 7 | Crohn's Disease | Acrodysostosis | Vitiligo | Dermatomyositis | Osteoporosis, Postmenopausal | Infantile Nephropathic Cystinosis | Beckwith-Wiedemann Syndrome | Alpha-mannosidosis | Binge Eating Disorder | Paroxysmal Kinesigenic Dyskinesia | Pfeiffer Syndrome | Pneumonia, Mycoplasma | Hereditary Coproporphyria | Tendinopathy | Cardiofaciocutaneous Syndrome | Hereditary Sensory Neuropathy Type 1 | Retinopathy Of Prematurity | Macrodactyly | Intermittent Claudication | Cervical Dystonia | Acute Coronary Syndrome | Chondrosarcoma | Aicardi-Goutieres Syndrome | Neurofibromatosis Type 2 | Chromosome 17q21.31 Deletion Syndrome | Lassa Fever | Albinism | Early Infantile Epileptic Encephalopathy 1 | Cerebral Amyloid Angiopathy | Farber Disease | Mucormycosis | Congenital Torticollis | Tyrosinemia Type 1 | Blau Syndrome | Olmsted Syndrome | Myoclonic Epilepsy With Ragged Red Fibers | Spinocerebellar Ataxia Type 16 | Hypotonia-cystinuria Syndrome | Cohen Syndrome | Familial Partial Lipodystrophy | Oculopharyngeal Muscular Dystrophy | Encephalopathy, Hepatic | Hereditary Xerocytosis | Behavioral Variant Of Frontotemporal Dementia | Carcinoid Syndrome | Alexander Disease | Dysplastic Nevus | Hepatorenal Syndrome | Leber Hereditary Optic Neuropathy | Myopathy | Tyrosine Hydroxylase Deficiency | Von Willebrand Disease | Acral Lentiginous Melanoma | Nutrition Disorders | Diabetes Type 1 | Crimean-Congo Hemorrhagic Fever | Congestive Heart Failure | Sertoli Cell-only Syndrome | Atelosteogenesis Type 2 | Cholangiocarcinoma | Ischemia | Glycogen Storage Disease Type 4 | Glycogen Storage Disease Type 1b | Familial Hyperaldosteronism | Familial Glucocorticoid Deficiency | Pre-eclampsia | Contact Dermatitis | Diabetic Neuropathy | Hyperinsulinemic Hypoglycemia | Hemolytic Anemia | Spondylo-ocular Syndrome | Spinal Muscular Atrophy Type 2 | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Multiple Sclerosis, Primary Progressive | Malignant Fibrous Histiocytoma | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Cerebellar Ataxia, Cayman Type | Waldenstrom Macroglobulinemia | GNE Myopathy | Treacher Collins Syndrome | Restless Legs Syndrome | Oral Lichen Planus | Hodgkin Lymphoma | Uremic Pruritus | Cheilitis