Blue Nevus

About the Disease
Ti猫che-Jadassohn Nevus, also known as blue nevus, is related to carney complex variant and blue nevi, familial multiple. An important gene associated with Ti猫che-Jadassohn Nevus is TBX5 (T-Box Transcription Factor 5). The drugs Miconazole and Sirolimus have been mentioned in the context of this disorder. Affiliated tissues include lymph node, skin and cervix.

Common Targets
GNAQ | TEK | CYSLTR2 | GNA11 | G673 | NRAS | PLCB4

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

Other Diseases

Alveolar Capillary Dysplasia | Pneumococcal Meningitis | Glaucoma, Congenital | Diabetes Insipidus, Nephrogenic | Vitreoretinopathy, Proliferative | Cranial Nerve Disease | TARP Syndrome | Aplasia Cutis Congenita | HELLP Syndrome | Spondylolisthesis | Carpal Tunnel Syndrome | Sarcoma | Poirier-Bienvenu Neurodevelopmental Syndrome | Diffuse Mesangial Sclerosis | Spinocerebellar Ataxia Type 10 | X-linked Myotubular Myopathy | Intestinal Tuberculosis | Transient Bullous Dermolysis Of The Newborn | Progressive Myoclonic Epilepsy | Esophagitis, Eosinophilic | Paroxysmal Nocturnal Hemoglobinuria | Facioscapulohumeral Muscular Dystrophy Type 2 | Klinefelter Syndrome | Neurotoxicity | Autosomal Recessive Spastic Paraplegia Type 54 | Giant Cell Glioblastoma | Hepatopulmonary Syndrome | Bipolar Disorder | Congenital Adrenal Hyperplasia | PHARC Syndrome | Corneal Neovascularization | Spinocerebellar Ataxia Type 3 | Autism Spectrum Disorders | Renal Medullary Carcinoma | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Rheumatoid Arthritis | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Glomerulonephritis | Spermatocele | Hereditary Folate Malabsorption | Autoimmune Disease | Vitamin A Deficiency | Tremor | Monilethrix | Thrombotic Microangiopathy | Sleep Apnea, Central | Usher Syndrome Type I | Schizoaffective Disorder | Occipital Neuralgia | Peters-plus Syndrome | Acquired Partial Lipodystrophy | Swine Influenza | Lactose Intolerance | Hypospadias | Juvenile Myelomonocytic Leukemia | Neural Tube Defect | Schizencephaly | Stomatitis | Meningioma | Pneumonia, Mycoplasma | Blepharospasm | Oral Lichen Planus | ADNP Syndrome | Motion Sickness | Hoyeraal-Hreidarsson Syndrome | Heroin Dependence | Smith-Kingsmore Syndrome | Chronic Kidney Disease | Carcinoma, Merkel Cell | Gangliosidosis, GM1 | Trismus-pseudocamptodactyly Syndrome | Cholelithiasis | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Dentinogenesis Imperfecta | Osteogenesis Imperfecta Type III | Leri-Weill Dyschondrosteosis | Venous Insufficiency | Pancreatitis, Chronic | Leukoplakia, Oral | Long QT Syndrome Type 2 | Majeed Syndrome | Ileitis | Temtamy Preaxial Brachydactyly Syndrome | Neuroectodermal Tumors, Primitive | Borderline Personality Disorder | Diamond-Blackfan Anemia | Eclampsia | Ectrodactyly | Megaloblastic Anemia | Zollinger-Ellison Syndrome | Spinocerebellar Ataxia Type 6 | Retinal Dystrophy | Osmotic Demyelination Syndrome | Glutathione Synthetase Deficiency | Wolfram Syndrome 2 | Hairy Cell Leukemia | Bietti Crystalline Dystrophy | Persistent Truncus Arteriosus | Tetanus | Autonomic Nervous System Disorders | Wiskott-Aldrich Syndrome | Rhizomelic Chondrodysplasia Punctata | Beta-Propeller Protein-associated Neurodegeneration | Acrodysostosis | Panic Disorder | Carotid Artery Disease | Rheumatic Heart Disease | Alpers Syndrome | Oculocutaneous Albinism Type 2 | Familial Cerebral Amyloid Angiopathy | Diabetic Encephalopathy | Hyperlipidemia Type V | Pearson Syndrome | Pontocerebellar Hypoplasia | Dysequilibrium Syndrome | Glycogen Storage Disease Type 4 | Spinocerebellar Ataxia Type 38 | Tyrosinemia Type 1 | Multiple System Atrophy | Supravalvular Aortic Stenosis | Pituitary Disorders | Infertility, Male | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Vulvovaginitis | Cantu Syndrome | Primary Erythromelalgia | ICF Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Kleine-Levin Syndrome | Mannosidase Deficiency Diseases | Bloom Syndrome | Heart Block | Hemorrhoids | Erectile Dysfunction | Blepharo-cheilo-odontic Syndrome | Porphyria | Cleidocranial Dysplasia | Panniculitis | Fukuyama Congenital Muscular Dystrophy | Milk Allergy | Sick Sinus Syndrome 1 | Colitis, Collagenous | Neuromyelitis Optica | Amyotrophic Lateral Sclerosis | Kidney Stones | Glioblastoma | Follicular Dendritic Cell Sarcoma | Diabetic Neuropathy | Erysipelas | Thyroid Dyshormonogenesis | Gastric Atrophy | Renal Tubular Acidosis | Acanthosis Nigricans | Alopecia Totalis | Ichthyosis, X-linked | Hepatitis B, Chronic | Ebstein Anomaly | Lipoma | Thrombophilia | GLUT1 Deficiency Syndrome | Rift Valley Fever | Acromesomelic Dysplasia | CHOPS Syndrome | Papilledema | Mucolipidosis Type IV | Adenoid Cystic Carcinoma | Adenoma, Villous | Centronuclear Myopathy | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Galactosemia | Familial Hyperaldosteronism | Tetraplegia | Polydactyly | Bare Lymphocyte Syndrome | Corneal Dystrophy | Intracerebral Hemorrhage | Agnathia-Otocephaly Complex | Isobutyryl-CoA Dehydrogenase Deficiency | Behcet's Disease | Heart Failure | Hepatoblastoma | Fibrosarcoma | LEOPARD Syndrome | Sclerosteosis | Neurofibromatosis Type 1 | Congenital Hypofibrinogenemia | Hepatic Adenomatosis | Aneurysm, Abdominal Aortic | Walker-Warburg Syndrome | Cerebrovascular Disorders | Jawad Syndrome | Dysmorphophobia | Shprintzen-Goldberg Syndrome | Open-angle Glaucoma | Isovaleric Acidemia | Congenital Lipoid Adrenal Hyperplasia | Chronic Thromboembolic Pulmonary Hypertension | Leukoplakia | Uremic Pruritus | Lattice Corneal Dystrophy | Cholestasis, Intrahepatic | Dysfibrinogenemia | Alkaptonuria | Retinoblastoma | Sarcosinemia | Dyskeratosis Congenita | Cornelia De Lange Syndrome | Endophthalmitis | Neurodevelopmental Disorders | Plasma Cell Dyscrasia | Hypoplastic Left Heart Syndrome | Purpura, Thrombotic Thrombocytopenic | Achondrogenesis | Shock, Cardiogenic | Xeroderma Pigmentosum | Neurocysticercosis | Hemolytic Anemia | Non-small Cell Lung Cancer | Birk-Barel Syndrome | Retinitis Pigmentosa 3 | Cousin Syndrome | Asphyxia Neonatorum | Apraxia | Spinocerebellar Ataxia Type 1 | Pernicious Anemia | Lymphangioma | Cutaneous Mastocytosis | Benign Recurrent Intrahepatic Cholestasis 1 | Melanoma, Uveal | Non-Hodgkin Lymphoma | Skin Fragility-woolly Hair Syndrome | Episodic Ataxia Type 2 | Roberts Syndrome | Keratosis, Seborrheic | Congenital Nystagmus | Sialoadenitis | Tietze Syndrome | Chronic Lymphocytic Leukemia | Inflammatory Myofibroblastic Tumor | Genitopatellar Syndrome | Temporal Lobe Epilepsy | Thrombosis | Hereditary Multiple Exostoses | Peeling Skin Syndrome Type B | Arteriosclerosis | Cocaine-Related Disorders | Ocular Hypertension | Frank-ter Haar Syndrome | Mountain Sickness | Spinal Muscular Atrophy | Hereditary Spastic Paraplegia | Japanese Encephalitis | Prader-Willi Syndrome | Myhre Syndrome | Myopathy | Colon Adenoma | Pyoderma Gangrenosum | Lipid Storage Diseases | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Anorectal Fistula | Bone Marrow Necrosis | Alstrom Syndrome | Intestinal Hypomagnesemia 1 | Liebenberg Syndrome | Heterotaxy | Cerebrotendinous Xanthomatosis | Demyelinating Diseases | Paget's Disease Of The Breast | Lymphangioleiomyomatosis | Congenital Myasthenic Syndrome | Malonyl-CoA Decarboxylase Deficiency | Carcinoma, Transitional Cell | Still Disease | Pineoblastoma | Ganglioglioma | Autosomal Recessive Spastic Paraplegia Type 75 | Acute Leukemia | Lissencephaly 2 | Niemann-Pick Disease, Type C | Atrial Septal Defect | Cramp Fasciculation Syndrome | Niemann-Pick Disease, Type A | Waardenburg Syndrome Type 4 | Autoimmune Autonomic Ganglionopathy | Whipple's Disease | COACH Syndrome | Trachoma | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | T-cell Lymphoma, Subcutaneous Panniculitis-like | Lymphangiomatosis | Goiter, Nodular | Hyperthyroidism | Ovarian Hyperstimulation Syndrome | Lymphedema | Sialidosis | Infantile Refsum Disease | Dermatofibrosarcoma | Diabetes Type 2 | Babesiosis | Hydrocephalus | Leishmaniasis, Visceral | Sensorineural Hearing Loss | Encephalocele | Kabuki Syndrome 2 | Generalized Epilepsy With Febrile Seizures Plus | Mucolipidosis | Ichthyosis Hystrix, Curth-Macklin Type | Situs Inversus | Postpoliomyelitis Syndrome | Unverricht-Lundborg Syndrome | Muscular Dystrophy | Vaginitis | Mitochondrial Cytopathy | Melanoma, Malignant | Arthritis | Coloboma | Spinocerebellar Ataxia Type 14 | Cholestasis | Neuromyotonia | Schnitzler Syndrome | Stroke, Hemorrhagic | Adenoma, Pleomorphic | Ectopia Lentis, Isolated, Autosomal Recessive | Dengue Shock Syndrome | Encephalitis | Lassa Fever | Cancer, Bladder | Creatine Deficiency Syndrome Due To AGAT Deficiency | Diabetes Type 1 | Hyperandrogenemia | Hyperkalemic Periodic Paralysis | Duchenne Muscular Dystrophy | Kallmann Syndrome | Meconium Ileus | Nasodigitoacoustic Syndrome | Glutaric Aciduria Type 2 | Chronic Neutrophilic Leukemia | Adenosine Deaminase 2 Deficiency | Eosinophilia | Hernia, Inguinal | Antley-Bixler Syndrome | Giant Axonal Neuropathy | Okihiro Syndrome | Platelet Disorders | Benign Familial Neonatal Convulsions | Obesity, Morbid | T-cell Prolymphocytic Leukemia | Insulinoma | Tumoral Calcinosis | Primary Hyperoxaluria | Schizotypal Personality Disorder | Delirium | Raynaud Phenomenon | Zellweger Syndrome | Intestinal Pseudo-obstruction | Infantile Liver Failure Syndrome 1 | VACTERL Association | Hamartoma | Sclerosing Cholangitis | Cavitary Optic Disc Anomalies | Premenstrual Syndrome | CHARGE Syndrome | Citrullinemia | Pseudohermaphroditism | Chromosome 17q21.31 Deletion Syndrome | Membranous Nephropathy | Tardive Dyskinesia | Hepatitis E | Inflammatory Myopathy | Discoid Lupus Erythematosus | Inborn Errors Of Metabolism | Left Ventricular Noncompaction | Hypertriglyceridemia | Optic Neuritis | Metachromatic Leukodystrophy | Tatton-Brown-Rahman Syndrome | Hypobetalipoproteinemias | Pericarditis | Tay-Sachs Disease | Lamellar Ichthyosis | Crohn's Disease | Oligodendroglioma | Pneumothorax | Aldosterone Deficiency | Budd-Chiari Syndrome | Anemia | Pityriasis Rubra Pilaris | Epithelial-myoepithelial Carcinoma | Muir-Torre Syndrome | Pleomorphic Xanthoastrocytoma | Enhanced S-cone Syndrome | Ischemia | Alzheimer Disease, Late Onset | Takotsubo Cardiomyopathy | Pterygium | Protein C Deficiency | Methemoglobinemia | Varicocele