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

LMNA-related Congenital Muscular Dystrophy | Avian Influenza | Tracheal Disorders | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Sleep Apnea, Central | Intestinal Hypomagnesemia 1 | Follicular Dendritic Cell Sarcoma | Keratitis-ichthyosis-deafness Syndrome | Spinocerebellar Ataxia Type 31 | Myositis, Focal | Glucagonoma | 3-methylglutaconic Aciduria Type I | Gnathodiaphyseal Dysplasia | Pituitary Dwarfism | Waardenburg Syndrome Type 1 | L-2-Hydroxyglutaric Aciduria | Astigmatism | Hartsfield Syndrome | Tendinitis | Pachyonychia Congenita | Fucosidosis | Spondylometaphyseal Dysplasia | Senior-Loken Syndrome | Chromosome 16p11.2 Deletion Syndrome | Trigonocephaly | FG Syndrome | N-acetylglutamate Synthase Deficiency | Papilloma | Usher Syndrome Type I | Fowler's Syndrome | Leishmaniasis, Cutaneous | Ligneous Conjunctivitis | Mitochondrial DNA Depletion Syndrome | Light Chain Amyloidosis | Glycogen Storage Disease Type 5 | Megalencephaly | Snyder-Robinson Syndrome | Agoraphobia | Tibial Muscular Dystrophy | Shprintzen-Goldberg Syndrome | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Nemaline Myopathy | Insulin Resistance | Pontocerebellar Hypoplasia Type 2 | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Leukodystrophies | Kashin-Beck Disease | Metabolic Syndrome | Pseudohypoparathyroidism Type 1B | Vertebrobasilar Insufficiency | Discoid Lupus Erythematosus | Weill-Marchesani Syndrome | Precocious Puberty | Hypertelorism | Stuttering | Charcot-Marie-Tooth Disease, Type 1A | Blepharoconjunctivitis | Gingivitis | Recurrent Respiratory Papillomatosis | NDH Syndrome | Dominant Optic Atrophy | Erythrokeratodermia Variabilis | Paget's Disease Of The Breast | Werner's Syndrome | Wolfram Syndrome | Chitayat Syndrome | Crouzon Syndrome With Acanthosis Nigricans | Localized Scleroderma | Alveolar Capillary Dysplasia | Knobloch Syndrome | Progressive Familial Intrahepatic Cholestasis | Delayed Sleep Phase Syndrome | Inflammatory Joint Disease | Liebenberg Syndrome | Alopecia | Torticollis | DOCK8 Immunodeficiency Syndrome | Spondylocostal Dysostosis | Autoimmune Autonomic Ganglionopathy | Gynecomastia | Basan Syndrome | Cardiofaciocutaneous Syndrome | Intermittent Explosive Disorder | Netherton Syndrome | Intestinal Pseudo-obstruction | Osteogenesis Imperfecta Type III | Tumoral Calcinosis | Small Lymphocytic Lymphoma | Endocarditis | Waardenburg Syndrome Type 2E | Pneumonia, Bacterial | Iron Deficiency Anemia | Erythema Nodosum | Primary Progressive Nonfluent Aphasia | Hereditary Pyropoikilocytosis | Insulinoma | Common Cold | Osteogenesis Imperfecta Type II | Pigment Dispersion Syndrome | Joubert Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Clouston Hidrotic Ectodermal Dysplasia | Kidney Stones | Larsen Syndrome | Lymphoma, Follicular | Lupus Erythematosus | Sitosterolemia | Cystitis | Hereditary Spherocytosis | Lymphangioleiomyomatosis | Focal Segmental Glomerulosclerosis | Cyclic Vomiting Syndrome | Hypersensitivity | Vertigo | Hypertriglyceridemia | Nevus | Sarcoma, Ewing | Diabetes Insipidus, Neurogenic | Autism | Creatine Deficiency Syndrome Due To AGAT Deficiency | Hypotonia-cystinuria Syndrome | Inborn Errors Of Metabolism | Congenital Aniridia | Arthritis, Reactive | Nanophthalmos | Dementia, Vascular | Parkinson Disease 6, Autosomal Recessive Early-onset | Amelanotic Melanoma | Usher Syndrome Type IIC | Anti-NMDA Receptor Encephalitis | Leukemia | Asphyxia Neonatorum | Central Retinal Artery Occlusion | 3-hydroxy-3-methylglutaric Aciduria | Hamartoma | Encephalopathy, Glycine | Lymphoma, B-cell | Neurofibroma, Plexiform | Craniopharyngioma | Compartment Syndrome | Poikiloderma With Neutropenia | Bernard-Soulier Syndrome | Cardiomyopathy, Restrictive | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Chronic Granulomatous Disease, X-linked | Neurogenic Bladder | Ameloblastoma | Genee-Wiedemann Syndrome | Gout | Smith-Magenis Syndrome | Melanoma, Malignant | Tyrosinemia Type 1 | Wolman Disease | Acute Motor Axonal Neuropathy | Double Outlet Right Ventricle | Bicuspid Aortic Valve | Familial Male-limited Precocious Puberty | Coronary Heart Disease | Waardenburg Syndrome Type 2A | Myoclonus-dystonia Syndrome | Papulopustular Rosacea | CREST Syndrome | Holt-Oram Syndrome | Biotinidase Deficiency | Cherubism | Cousin Syndrome | Chromosome 5q Deletion Syndrome | Hepatopulmonary Syndrome | Ehlers-Danlos Syndrome | Hermansky-Pudlak Syndrome | Cervicitis | Specific Granule Deficiency | Cellulitis | Hypercholesterolemia | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Parvovirus B19 Infection | Angioedema | Nail-Patella Syndrome | Arthritis, Psoriatic | Hypothyroidism | Pulmonary Alveolar Proteinosis | Apparent Mineralocorticoid Excess Syndrome | Desbuquois Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Lyme Disease | Vestibular Disease | Phenylketonuria | Primary Biliary Cholangitis | Olmsted Syndrome | Okihiro Syndrome | Hyperammonemia | Charcot-Marie-Tooth Disease, Type 2C | Acute Tubular Necrosis | Gerstmann-Straussler-Scheinker Syndrome | Hyperferritinemia-cataract Syndrome | Sarcosinemia | Angioimmunoblastic T-cell Lymphoma | Retinitis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Early Infantile Epileptic Encephalopathy 13 | Chronic Beryllium Disease | Onchocerciasis | Nephrosclerosis | Familial Mediterranean Fever | Achromatopsia | Open-angle Glaucoma | Hemolytic Uremic Syndrome | Mucormycosis | Harlequin Ichthyosis | Sialoadenitis | Contact Dermatitis | Charcot-Marie-Tooth Disease, Type 6 | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Hemolytic Uremic Syndrome, Atypical | Antenatal Bartter Syndrome Type 1 | Huntington's Disease-like 2 | Occipital Neuralgia | Frank-ter Haar Syndrome | NGLY1 Deficiency | Peutz-Jeghers Syndrome | Infantile Spasm | Neuroleptic Malignant Syndrome | Impetigo | Moyamoya Disease | Hidradenitis Suppurativa | Astrocytoma | Zellweger Syndrome | Uveitis | Atelosteogenesis Type 2 | Vogt-Koyanagi-Harada Syndrome | Gastric Atrophy | Retinal Dystrophy, Early-onset Severe | Oligospermia | Anxiety Disorders | Potocki-Shaffer Syndrome | Malonyl-CoA Decarboxylase Deficiency | Polycythemia Vera | Teratozoospermia | Wilson's Disease | Autosomal Recessive Bestrophinopathy | Adenomatoid Tumor | Tyrosinemia Type 2 | Macrophagic Myofasciitis | Apraxia | Woodhouse-Sakati Syndrome | Intracranial Hypertension | Menkes Disease | Cancer, Kidney | Spermatocele | Acne | Spondyloperipheral Dysplasia | Lymphangioma | Thalassemia | Parkinson's Disease | Multisystemic Smooth Muscle Dysfunction Syndrome | Herpes Genitalis | Periodic Limb Movement Disorder | Autoimmune Disease | Cardiomyopathy, Peripartum | Jawad Syndrome | Oculocutaneous Albinism | Sclerocornea | Lentigo | Essential Fructosuria | Charcot-Marie-Tooth Disease, Type 2A | Porphyria, Acute Intermittent | Synovitis | Gallstones | Cryptosporidiosis | Metachondromatosis | Paracoccidioidomycosis | Dental Caries | Carbamoyl Phosphate Synthetase I Deficiency | Osteochondrosis | Otopalatodigital Syndrome Type 2 | Frontotemporal Dementia | Familial Digital Arthropathy-brachydactyly | Fetal Akinesia Deformation Sequence | Infertility | Leukoencephalopathy, Progressive Multifocal | Pelizaeus-Merzbacher Disease | Tatton-Brown-Rahman Syndrome | Erythema Multiforme | Lymphoproliferative Disorders | Micro Syndrome | Pyelonephritis | Sleep Apnea | Lactose Intolerance | Inflammatory Myofibroblastic Tumor | Pierpont Syndrome | Schistosomiasis | Borderline Personality Disorder | Aceruloplasminemia | Prune Belly Syndrome | Actinomycetoma | Acrodermatitis | Pulmonary Vein Stenosis | Hereditary Spastic Paraplegia | Meier-Gorlin Syndrome | Chronic Neutrophilic Leukemia | Chanarin-Dorfman Syndrome | Ischemia | Osteochondroma | Retinopathy Of Prematurity | Bloom Syndrome | Giant Axonal Neuropathy | Spondylocarpotarsal Synostosis Syndrome | Progressive External Ophthalmoplegia | VEXAS Syndrome | Hyperprolactinemia | Keloid | Cirrhosis | Paternal Uniparental Disomy Of Chromosome 14 | Carcinoma, Merkel Cell | Familial Partial Lipodystrophy | Primary Hyperoxaluria | Wiskott-Aldrich Syndrome | Amelogenesis Imperfecta | Tylosis With Esophageal Cancer | Pontocerebellar Hypoplasia Type 7 | Anuria | Brugada Syndrome 1 | Anosmia, Congenital | Sotos Syndrome | Barakat Syndrome | Congenital Absence Of Vas Deferens | Vitiligo | Congenital Myasthenic Syndrome | Epidermolysis Bullosa Simplex, Generalized | Methemoglobinemia | Dengue Shock Syndrome | Craniofrontonasal Syndrome | Pelvic Inflammatory Disease | Schaaf-Yang Syndrome | Hyperkeratosis | Nicotine Dependence | Donnai-Barrow Syndrome | Greig Cephalopolysyndactyly Syndrome | Eosinophilic Asthma | Basal Ganglia Disease | Paronychia | Hemochromatosis Type 2 | Glaucoma, Congenital | Mycosis Fungoides | Multiple Myeloma | Lymphoma, Mantle Cell | Myoclonic Epilepsy With Ragged Red Fibers | Leber Hereditary Optic Neuropathy | Hepatitis B, Chronic | Dermatitis | SAPHO Syndrome | Glycogen Storage Disease Type 1b | Rothmund-Thomson Syndrome | Cluster Headache | Fahr Disease | Cerebrotendinous Xanthomatosis | Granuloma Annulare | Central Pain Syndrome | Pulmonary Sclerosing Hemangioma | Keratoconjunctivitis | Neuromuscular Disorders | Primary Hyperoxaluria Type 1 | Peters-plus Syndrome | Twin-to-twin Transfusion Syndrome | Exocrine Pancreatic Insufficiency | Pseudohermaphroditism | Adenocarcinoma | Galloway-Mowat Syndrome | Muscle Wasting | Synpolydactyly | Osteoarthritis | Sarcoma, Endometrial Stromal | Irritable Bowel Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Glycogen Storage Disease Type 4 | Plasma Cell Leukemia | Keratosis | Guillain-Barre Syndrome | Cutis Laxa | Myofibrillar Myopathy | Kleine-Levin Syndrome | Epidermolysis Bullosa Simplex, Localized | Walker-Warburg Syndrome | Methemoglobinemia Type IV | Congenital Dyserythropoietic Anemia Type 1 | Transcobalamin Deficiency | PASLI Disease | Geleophysic Dysplasia | Encephalocele | Kabuki Syndrome 2 | Charcot-Marie-Tooth Disease Type 2D | Trismus-pseudocamptodactyly Syndrome | Epithelioid Hemangioma | Dysplastic Nevus | Chronic Periodontitis | Congenital Adrenal Hyperplasia 1 | Maternally Inherited Diabetes And Deafness | Diabetes Gestational | CHOPS Syndrome | Melanoma