Tumoral Calcinosis

About the Disease
Tumoral Calcinosis, Hyperphosphatemic, Familial, 1, also known as hyperphosphatemic familial tumoral calcinosis, is related to hyperostosis and hypercalcemia, infantile, 1. An important gene associated with Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 is GALNT3 (Polypeptide N-Acetylgalactosaminyltransferase 3), and among its related pathways/superpathways are Disease and Signaling by Receptor Tyrosine Kinases. The drugs Salmon calcitonin and Calcitonin gene-related peptide have been mentioned in the context of this disorder. Affiliated tissues include bone, skin and eye, and related phenotypes are bone pain and periarticular subcutaneous nodules

Common Targets
ATP8A2 | LIAS | GALNT3 | ACSF2 | DNAH2 | FGF23 | HGS | DNAH17 | FBXO38 | CDH19 | SDK2 | GRK5 | KL | COX8C | TFF2 | ANXA2 | OR1J4

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

Other Diseases

Gastroschisis | Oculocutaneous Albinism Type 2 | Vestibular Disease | Dystonia Musculorum Deformans | Centronuclear Myopathy | Nail-Patella Syndrome | Polycystic Kidney, Autosomal Dominant | Hemimegalencephaly | Geleophysic Dysplasia | Neuromyelitis Optica | Porphyria, Variegate | Phosphoglycerate Dehydrogenase Deficiency | Papillon-Lefevre Syndrome | Cataract | Thrombasthenia | Hemorrhage | Mitochondrial Disease | Congenital Bile Acid Synthesis Defect | L-2-Hydroxyglutaric Aciduria | Thyroid Dysgenesis | Glutaric Aciduria Type 1 | Familial Isolated Hyperparathyroidism | Hypervalinemia | Diabetes Type 1 | Sick Sinus Syndrome | Megalencephaly | Goldenhar Syndrome | Erythropoietic Protoporphyria | Bruck Syndrome | Nemaline Myopathy | Waardenburg Syndrome Type 2A | Dengue Shock Syndrome | Blue Rubber Bleb Nevus Syndrome | Leishmaniasis, Cutaneous | Osmotic Demyelination Syndrome | Astrocytoma, Anaplastic | Trichothiodystrophy | Autoimmune Disease | Epidermodysplasia Verruciformis | Carbonic Anhydrase VA Deficiency | Homocystinuria | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Neurodevelopmental Disorders | Pure Red Cell Aplasia | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Hepatitis B, Chronic | Diabetic Neuropathy | B-cell Chronic Lymphocytic Leukemia | Cancer, Skin | Congenital Absence Of Vas Deferens | Colitis, Microscopic | Hypertension, Pulmonary | Hemangioma | Dengue Hemorrhagic Fever | Duodenal Atresia | Isovaleric Acidemia | Malignant Fibrous Histiocytoma | Molybdenum Cofactor Deficiency | Tyrosinemia | Meniere's Disease | Intestinal Obstruction | Epilepsy Of Infancy With Migrating Focal Seizures | Progressive Osseous Heteroplasia | Persistent Fetal Circulation | Orotic Aciduria | Esophageal Motility Disorders | Coloboma | Osteochondrosis | Familial Digital Arthropathy-brachydactyly | Porphyria, Acute Intermittent | Myoclonic Atonic Epilepsy | Progressive Encephalopathy-optic Atrophy Syndrome | CEDNIK Syndrome | Biotinidase Deficiency | Macrophagic Myofasciitis | Glycogen Storage Disease Type 6 | Glomerulonephritis | Amish Infantile Epilepsy Syndrome | Ectodermal Dysplasia | Autoimmune Polyendocrinopathy Syndrome Type I | Spinocerebellar Ataxia Type 15 | Overactive Bladder | Porphyria Cutanea Tarda | Liebenberg Syndrome | Palmoplantar Keratoderma | Malignant Peripheral Nerve Sheath Tumor | Spinal Muscular Atrophy | Pancytopenia | Pitt-Hopkins Syndrome | Hepatitis, Chronic | Primary Sclerosing Cholangitis | Saethre-Chotzen Syndrome | 3-M Syndrome | Prolactinoma | Gaucher Disease | Spondylocarpotarsal Synostosis Syndrome | Retinal Degeneration | Hyperparathyroidism, Primary | Fucosidosis | Retinal Coloboma | Hyperbilirubinemia, Neonatal | Spinocerebellar Ataxia Type 27 | Erythrokeratodermia Variabilis | Prader-Willi Syndrome | Sarcoidosis, Pulmonary | Inflammatory Joint Disease | Primary Aldosteronism | Parkinsonism | Maple Syrup Urine Disease | Renal Dysplasia | Peroxisomal Disorder | Fabry's Disease | Keratosis, Actinic | Intellectual Disability, Autosomal Dominant 5 | Oculocutaneous Albinism | Supravalvular Aortic Stenosis | Tetraplegia | Graves Disease | Strabismus | Congenital Mirror Movements | Nevus | Plasma Cell Leukemia | Anal Fissure | Mountain Sickness | Diabetes Gestational | Acute Lymphocytic Leukemia | Exocrine Pancreatic Insufficiency | Fahr Disease | Klippel-Feil Syndrome | Cousin Syndrome | Asphyxia Neonatorum | Esophagitis, Eosinophilic | Dystrophy, Cone-rod | Corneal Ulcer | Porencephaly | Stiff-man Syndrome | Choroiditis | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Alzheimer Disease, Late Onset | Anorchia | Focal Cortical Dysplasia Type 2 | Pseudohermaphroditism | Autoimmune Polyendocrine Syndrome | Pycnodysostosis | Wilson's Disease | Anorectal Fistula | Dermatomyositis | Sarcoma | Progressive Familial Intrahepatic Cholestasis | Cancer, Prostate | Oculocutaneous Albinism Type 4 | Brugada Syndrome 1 | Chronic Lymphocytic Leukemia | Hypertension, Renal | Pantothenate Kinase-associated Neurodegeneration | Spastic Paraplegia Type 7 | Chromosome 8q21.11 Deletion Syndrome | Colitis | Arteriovenous Malformations | Coffin-Lowry Syndrome | Kindler Syndrome | Hypohidrotic Ectodermal Dysplasia | Varicocele | Mosaic Variegated Aneuploidy Syndrome 2 | Sialoadenitis | Histiocytic Sarcoma | Bethlem Myopathy | Diffuse Palmoplantar Keratoderma | Multiple Hamartoma Syndrome | Chromosome 17q21.31 Deletion Syndrome | McLeod Syndrome | GATA2 Deficiency | Anorectal Malformations | Pendred Syndrome | Bipolar Disorder | Facioscapulohumeral Muscular Dystrophy Type 1 | Amyloidosis | Spinocerebellar Ataxia Type 7 | Primary Hyperoxaluria Type 1 | Glycogen Storage Disease Type 9 | Mucolipidosis Type II | Ichthyosis | Donnai-Barrow Syndrome | Acrocallosal Syndrome | Pigment Dispersion Syndrome | Werner's Syndrome | Sitosterolemia | Primary Familial Brain Calcification | Pulmonary Stenosis | Persistent Truncus Arteriosus | Retinoschisis | Osteochondroma | Renal Medullary Carcinoma | Perivascular Epithelioid Cell Tumor | Aspartylglycosaminuria | Optic Atrophy 2 | Gout | Cellulitis | Oculocutaneous Albinism Type 1 | Crimean-Congo Hemorrhagic Fever | COACH Syndrome | Macrodactyly | Neurodermatitis | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Acute Lung Injury | Parkinson's Disease | Basal Ganglia Cerebrovascular Disease | Galactosialidosis | Warsaw Breakage Syndrome | Chronic Leukemia | Spinocerebellar Ataxia Type 8 | Open-angle Glaucoma | Small Lymphocytic Lymphoma | Hepatoblastoma | Sweet Syndrome | Cutis Laxa | Hepatic Steatosis | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Proteus Syndrome | Cat Eye Syndrome | Lymphedema | Triple A Syndrome | Juvenile Myelomonocytic Leukemia | Measles | Meningioma, Benign | Mitochondrial DNA Depletion Syndrome | Apparent Mineralocorticoid Excess Syndrome | Budd-Chiari Syndrome | Angioedema, Hereditary | Corticobasal Syndrome | Osteonecrosis Of The Jaw | Thanatophoric Dysplasia Type 1 | Anosmia, Congenital | Thymoma, Malignant | DNA Ligase IV Deficiency | Antiphospholipid Syndrome | Giant Cell Arteritis | Infantile Nephropathic Cystinosis | Hyperlipidemia Type V | Renal-hepatic-pancreatic Dysplasia | Herpes Simplex Dermatitis | Myopathy | Hepatopulmonary Syndrome | Perry Syndrome | Trichotillomania | Seborrheic Dermatitis | IgA Deficiency | Premenstrual Syndrome | Anti-glomerular Basement Membrane Disease | Chordoid Glioma | Zollinger-Ellison Syndrome | Galloway-Mowat Syndrome | Venous Insufficiency | Currarino Syndrome | Harlequin Ichthyosis | Hypokalemia | Adenomatoid Tumor | Raine Syndrome | Coronary Heart Disease | Autosomal Recessive Spastic Paraplegia Type 54 | Bardet-Biedl Syndrome | Leber Congenital Amaurosis | Ovarian Sex Cord-stromal Tumor | Megaloblastic Anemia | Bainbridge-Ropers Syndrome | Neuroma | Scleroderma | Spinocerebellar Ataxia Type 5 | Cataplexy | Robinow Syndrome | Mabry Syndrome | Hypersomnia | Spinocerebellar Ataxia Type 42 | Arthritis, Reactive | Barakat Syndrome | Blood Protein Disorders | Polycythemia | Transcobalamin Deficiency | Muir-Torre Syndrome | Lactose Intolerance | Acute Motor Axonal Neuropathy | Chromosome 9q34.3 Deletion Syndrome | Leukemia-lymphoma, Adult T-cell | 3-methylglutaconic Aciduria Type I | Acquired Partial Lipodystrophy | Obesity, Morbid | Hepatitis A | Infantile Liver Failure Syndrome 1 | Asperger Syndrome | Syphilis | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Leukoencephalopathy, Progressive Multifocal | Thyrotoxic Periodic Paralysis | Astrocytoma | Wolfram Syndrome 2 | Placenta Previa | Keratopathy | Multiple Sulfatase Deficiency | Polycythemia Vera | Botulism | Autism Spectrum Disorders | Hemorrhoids | Metaphyseal Chondrodysplasia, Schmid Type | Retinal Dystrophy, Early-onset Severe | Dubin-Johnson Syndrome | Bulimia Nervosa | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Tricho-hepato-enteric Syndrome | Primary Biliary Cholangitis | Adenosine Deaminase 2 Deficiency | Carpal Tunnel Syndrome | Congenital Generalized Lipodystrophy | Dystonia-parkinsonism, X-linked | Myelitis | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Spitzoid Melanoma | 5-oxoprolinase Deficiency | Exfoliative Dermatitis | Congenital Diaphragmatic Hernia | Renal Hypomagnesemia 3 | VEXAS Syndrome | GM2-gangliosidosis AB Variant | Micro Syndrome | Urethritis | Familial Hypertrophic Cardiomyopathy | Photosensitivity | Pulmonary Sclerosing Hemangioma | Vertigo | Cardiofaciocutaneous Syndrome | Diabetes Mellitus, Transient Neonatal | Renal Tubular Dysgenesis | Urticaria | HUPRA Syndrome | C3 Glomerulonephritis | Endometrial Hyperplasia | Myasthenia Gravis | Retinal Vasculitis | Guanidinoacetate Methyltransferase Deficiency | Cutaneous Lupus Erythematosus | Primary Ovarian Insufficiency | Diabetes Insipidus, Neurogenic | Corneal Edema | Cryptosporidiosis | Greig Cephalopolysyndactyly Syndrome | Apraxia | Pachyonychia Congenita | Actinomycetoma | Sclerocornea | Fragile X Syndrome | Rothmund-Thomson Syndrome | Cutaneous Mastocytosis | Hyperostosis | Pulmonary Tuberculosis | Thrombocytopenia | Schwannomatosis | Meconium Ileus | Systemic Lupus Erythematosus | Glioma | Avian Influenza | Nephropathy | Nasodigitoacoustic Syndrome | Basal Ganglia Disease | Synpolydactyly | Glutathione Synthetase Deficiency | Bartter Syndrome | Anemia | Ornithine Transcarbamylase Deficiency | Antisocial Personality Disorder | Pneumothorax | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Hereditary Coproporphyria | Inflammatory Myofibroblastic Tumor | Carcinoid Syndrome | Craniofrontonasal Syndrome | Familial Hypobetalipoproteinemia | Onchocerciasis | Familial Thoracic Aortic Aneurysm | Hyperthermia, Malignant | Retinal Dystrophy | Dystonia | Osteosarcoma | Johanson-Blizzard Syndrome | Chorea-acanthocytosis | Schuurs-Hoeijmakers Syndrome | Acute Tubular Necrosis | Ataxia-ocular Apraxia 2 | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Spinocerebellar Ataxia Type 3 | Non-Langerhans Cell Histiocytosis | Distal Myopathy 2 | Insulin Resistance | Congenital Stromal Corneal Dystrophy | Endocarditis | Cockayne Syndrome | Cheilitis | Fibrosarcoma | Neurocysticercosis | Motion Sickness | Amelanotic Melanoma | Tyrosinemia Type 1