Disease

Heterotopic Ossification

About the Disease
Osseous Heteroplasia, Progressive, also known as progressive osseous heteroplasia, is related to myositis ossificans and ossification of the posterior longitudinal ligament of spine, and has symptoms including polydipsia and muscle weakness. An important gene associated with Osseous Heteroplasia, Progressive is GNAS (GNAS Complex Locus), and among its related pathways/superpathways are Signal Transduction and Akt Signaling. The drugs Etoricoxib and Cyclooxygenase 2 Inhibitors have been mentioned in the context of this disorder. Affiliated tissues include bone, skin and skeletal muscle, and related phenotypes are subcutaneous nodule and limitation of joint mobility

Common Targets
CASC20 | ACVR1 | TGFB1 | ACVRL1 | TGFB2 | Vascular endothelial growth factors (VEGF) (nonspecified subtype) | CTH | BMPR1A | TGFB3 | BMPR1B

疾病靶点研报
Heterotopic Ossification

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

Other Diseases

Focal Dermal Hypoplasia | Hepatitis E | Renal-hepatic-pancreatic Dysplasia | Lymphoproliferative Disorders | Binge Eating Disorder | 3-methylglutaconic Aciduria Type I | Wolcott-Rallison Syndrome | Fibrodysplasia Ossificans Progressiva | Nephropathy | Early Infantile Epileptic Encephalopathy | Central Core Disease | Urethritis | Hepatic Veno-occlusive Disease | Coffin-Siris Syndrome | Gyrate Atrophy Of The Choroid And Retina | Arteriovenous Malformations | Endometrial Hyperplasia | Retinal Coloboma | Charcot-Marie-Tooth Disease Type 2D | Adenosine Deaminase Deficiency | Allan-Herndon-Dudley Syndrome | Dysfibrinogenemia | Neurogenic Bladder | Tatton-Brown-Rahman Syndrome | Chronic Lymphocytic Leukemia | Brooke-Spiegler Syndrome | Tietze Syndrome | Kallmann Syndrome | Nemaline Myopathy | Creatine Deficiency Syndrome Due To AGAT Deficiency | Tyrosinemia | Veno-occlusive Disease | Brenner Tumor | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Stiff-man Syndrome | Spinocerebellar Ataxia Type 21 | Cyclic Vomiting Syndrome | Familial Hemiplegic Migraine | Chloridorrhea, Congenital | Epithelioid Hemangioma | CREST Syndrome | Fetal Akinesia Deformation Sequence | Wolff-Parkinson-White Syndrome | Camurati-Engelmann Disease | Low Tension Glaucoma | Goiter | Gynecomastia | Krabbe Disease | Cancer, Prostate | Encephalopathy | Charcot-Marie-Tooth Disease, Type 2C | Hartsfield Syndrome | Guillain-Barre Syndrome | Bartter Syndrome | Familial Hyperaldosteronism | Alpers Syndrome | Eclampsia | REM Sleep Behavior Disorder | Emery-Dreifuss Muscular Dystrophy | Polydactyly | Trimethylaminuria | Glycogen Storage Disease Type 1 | Wagner Disease | Tricho-hepato-enteric Syndrome | Vitamin D Deficiency | Spinocerebellar Ataxia Type 14 | Branchiootorenal Syndrome | Martsolf Syndrome | Melanoma | Hypohidrotic Ectodermal Dysplasia, X-linked | Obesity, Morbid | Sezary Syndrome | Amblyopia | Lymphoma, Mantle Cell | Sponastrime Dysplasia | Lipoma | Oculodentodigital Dysplasia | Glioma | Toxoplasmosis | Hyperphenylalaninemia | Osteogenesis Imperfecta Type III | Kleine-Levin Syndrome | Rickets | Argininosuccinic Aciduria | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Diabetes Type 2 | Smoldering Myeloma | Macular Corneal Dystrophy | Paraganglioma | Carcinoid Syndrome | Oculocutaneous Albinism Type 1 | Bruck Syndrome | Angioedema, Acquired | Nephroblastoma | Myelomeningocele | Rubeosis Iridis | Traboulsi Syndrome | IgA Nephropathy | Congenital Afibrinogenemia | D-2-Hydroxyglutaric Aciduria | Bare Lymphocyte Syndrome | Cerebral Cavernous Malformations | Lung Diseases | Hypothalamic Obesity | Giant Cell Arteritis | Kabuki Syndrome | Cyst | Facioscapulohumeral Muscular Dystrophy | Craniofrontonasal Syndrome | Pulmonary Sclerosing Hemangioma | Congestive Heart Failure | Impetigo | Multiple Epiphyseal Dysplasia | Alzheimer Disease, Late Onset | Hypophosphatasia | Nephrosclerosis | Gestational Trophoblastic Disease | Intestinal Tuberculosis | Cranial Nerve Disease | HIBCH Deficiency | Metachromatic Leukodystrophy | Multisystemic Smooth Muscle Dysfunction Syndrome | Blepharophimosis Syndrome | Oligospermia | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Menetrier Disease | Dysmorphophobia | Behavioral Variant Of Frontotemporal Dementia | Dermatitis | Endophthalmitis | Fuchs Heterochromic Iridocyclitis | Fetal And Neonatal Alloimmune Thrombocytopenia | Von Hippel-Lindau Disease | Plasma Cell Leukemia | Wiskott-Aldrich Syndrome | Hodgkin Lymphoma | Chylothorax, Congenital | Bone Giant Cell Tumor | Mumps | Loeys-Dietz Syndrome | Neurofibromatosis-Noonan Syndrome | Steel Syndrome | Osteochondroma | Apert Syndrome | Parvovirus B19 Infection | Porphyria, Variegate | Asthma, Exercise-induced | Anosmia, Congenital | Inflammatory Myopathy | Congenital Tufting Enteropathy | Mucolipidosis Type III | Hemochromatosis Type 2 | Thrombasthenia | Juvenile Myelomonocytic Leukemia | Lattice Corneal Dystrophy | Alopecia Areata | Alopecia Totalis | Schnyder Crystalline Corneal Dystrophy | Duane Retraction Syndrome | Glomerulonephritis | Optic Neuritis | Lymphangioma | Ocular Hypertension | Diabetes Insipidus, Nephrogenic | Hypogammaglobulinemia | Vici Syndrome | Non-small Cell Lung Cancer | Prader-Willi Syndrome | Jalili Syndrome | Meleda Disease | Granular Corneal Dystrophy | Waldenstrom Macroglobulinemia | Erysipelas | Chromosome 8q21.11 Deletion Syndrome | Agranulocytosis | Hyperbilirubinemia, Neonatal | Glomerulonephritis, Membranous | Varicocele | Inflammatory Bowel Disease | Anuria | Optic Neuropathy, Anterior Ischemic | Hyper IgE Syndrome | Salla Disease | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Osmotic Demyelination Syndrome | Hepatitis, Chronic | Cerebrovascular Disorders | Ocular Albinism Type 1 | Neurofibroma | Meniere's Disease | Retinal Dystrophy, Early-onset Severe | Short-chain Acyl-CoA Dehydrogenase Deficiency | Sarcoma, Ewing | Papulopustular Rosacea | Prolidase Deficiency | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Mucolipidosis Type IV | Otopalatodigital Syndrome Type 2 | Malaria | Episodic Ataxia Type 2 | Thrombocytopenia | Hyperkeratosis | Hypertensive Nephropathy | Mucolipidosis | Melanocytic Nevus | Spinocerebellar Ataxia Type 15 | Pendred Syndrome | Multiple Sulfatase Deficiency | Stroke | Nephritis, Interstitial | Crouzon Syndrome With Acanthosis Nigricans | Exotropia | Pterygium | Waardenburg Syndrome Type 2A | Enlarged Vestibular Aqueduct | Acrodermatitis Enteropathica | Spinal Muscular Atrophy Type 3 | Dyggve-Melchior-Clausen Disease | Asphyxia Neonatorum | Dowling-Degos Disease | Congenital Dysfibrinogenemia | Early Infantile Epileptic Encephalopathy 13 | Polymyalgia Rheumatica | Hepatic Adenomatosis | Lymphoma | Genitopatellar Syndrome | Pneumococcal Meningitis | Discoid Lupus Erythematosus | Familial Digital Arthropathy-brachydactyly | Congenital Stationary Night Blindness | Progressive Encephalopathy-optic Atrophy Syndrome | Botulism | Multiple Myeloma | Glomerulonephritis, Membranoproliferative | Cystitis, Interstitial | Usher Syndrome Type IIC | Amelanotic Melanoma | Medulloblastoma | Schistosomiasis | Feingold Syndrome | Placenta Previa | Non-Hodgkin Lymphoma | Craniolenticulosutural Dysplasia | Lupus Erythematosus | Osteonecrosis | Panniculitis | Babesiosis | 5-oxoprolinase Deficiency | Episodic Ataxia | Williams Syndrome | Carey-Fineman-Ziter Syndrome | Cabezas Syndrome | Orthostatic Intolerance | CDKL5 Deficiency Disorder | Rotor Syndrome | Hypospadias | Retinoschisis | ACTH-independent Macronodular Adrenal Hyperplasia | Localized Scleroderma | Charcot-Marie-Tooth Disease Type 2T | Neurotoxicity | Spinocerebellar Ataxia Type 17 | Hypertension, Renal | Tuberculosis | Hypertension, Renovascular | Schwartz-Jampel-Aberfeld Syndrome | Lymphangioleiomyomatosis | Scapuloperoneal Myopathy, X-linked Dominant | DNA Ligase IV Deficiency | Spondylocostal Dysostosis | Familial Partial Lipodystrophy | Thrombocythemia, Essential | Speech Disorders | Prolymphocytic Leukemia | Colitis, Lymphocytic | Cardiofaciocutaneous Syndrome | Parkinson's Disease | Sarcoma | Gout | Restless Legs Syndrome | Thyroid Dyshormonogenesis | Progressive Familial Intrahepatic Cholestasis Type 1 | Schnitzler Syndrome | Leukoplakia, Oral | Dent Disease | Seborrheic Dermatitis | Shwachman-Bodian-Diamond Syndrome | Cousin Syndrome | Myosin Storage Myopathy | Measles | Sensorineural Hearing Loss | Myofibrillar Myopathy | 3-methylcrotonyl-CoA Carboxylase Deficiency | Meckel-Gruber Syndrome | Thalassemia | Hypertension | Epiphyseal Chondrodysplasia, Miura Type | Corneal Dystrophy And Perceptive Deafness | Coffin-Lowry Syndrome | Dwarfism | Lattice Corneal Dystrophy Type 1 | Reticular Dysgenesis | Cranioectodermal Dysplasia | Congenital Disorders Of Glycosylation | Incontinentia Pigmenti | Muscular Dystrophy | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Language Disorders | Hyperferritinemia-cataract Syndrome | Heimler Syndrome | Large Granular Lymphocytic Leukemia | Meconium Ileus | NDH Syndrome | Ventricular Septal Defect | Hypercholesterolemia | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Cardiomyopathy, Peripartum | Hyperlipidemia | Tendinitis | Anti-NMDA Receptor Encephalitis | Brachydactyly | Progressive Familial Intrahepatic Cholestasis Type 2 | Intestinal Obstruction | Lactose Intolerance | Saul-Wilson Syndrome | GLUT1 Deficiency Syndrome | Astrocytoma, Anaplastic | Hemorrhagic Disorders | Skin Carcinoma | Hypersensitivity Pneumonitis | Androgen Insensitivity | Cerebrotendinous Xanthomatosis | Cramp Fasciculation Syndrome | Long QT Syndrome Type 1 | Sensory Neuropathy | Takenouchi-Kosaki Syndrome | Hypertrophy | Cysticercosis | Thanatophoric Dysplasia | Hamartoma | Macrophage Activation Syndrome | Swine Influenza | Arthritis | Erythropoietic Protoporphyria | Chronic Enteropathy Associated With SLCO2A1 Gene | Parkinson Disease 6, Autosomal Recessive Early-onset | Combined Malonic And Methylmalonic Acidemia | Congenital Myasthenic Syndrome | Obsessive-compulsive Disorder | Eosinophilia | Nicotine Addiction | Arthropathy | Lymphoma, AIDS-related | Osteoporosis-pseudoglioma Syndrome | Acne | Coloboma | Thin Basement Membrane Disease | Noonan Syndrome-like Disorder With Loose Anagen Hair | Chronic Inflammatory Demyelinating Polyneuropathy | Coronary Restenosis | Craniosynostosis | Poirier-Bienvenu Neurodevelopmental Syndrome | Colitis, Collagenous | Hepatopulmonary Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Chylomicron Retention Disease | Borderline Personality Disorder | Focal Cortical Dysplasia Type 2 | Rift Valley Fever | Micropenis | Hypoplastic Left Heart Syndrome | Intermittent Claudication | Dyslexia | Epidermolytic Ichthyosis, Annular | Neurocutaneous Melanocytosis | Eiken Syndrome | Duodenal Atresia | Primary Progressive Aphasia | Fibronectin Glomerulopathy | Jaundice, Obstructive | Brugada Syndrome 1 | Phenylketonuria | Pneumonia, Mycoplasma | Progressive Familial Intrahepatic Cholestasis | Growth Hormone Excess | Keratitis | Antithrombin III Deficiency | Colon Adenoma | Diabetic Nephropathy | Non-epidermolytic Palmoplantar Keratoderma | Proteasome-associated Autoinflammatory Syndrome 2 | Walker-Warburg Syndrome | Opisthorchiasis | Meningitis | Cancer, Skin | Alagille Syndrome | Johanson-Blizzard Syndrome | Muckle-Wells Syndrome | Congenital Heart Defects | Corneal Ulcer