Amelanotic Melanoma

About the Disease
Amelanotic Melanoma, also known as melanoma, amelanotic, is related to albinism and oculocutaneous albinism. An important gene associated with Amelanotic Melanoma is TYR (Tyrosinase), and among its related pathways/superpathways are Neuroscience and Neural crest differentiation. Affiliated tissues include skin, lymph node and endothelial, and related phenotypes are no effect and no effect

Common Targets
TEF | LRMDA | POMC | TYR | SLC24A5 | KITLG | DIPK2A | HHEX | NELFB | TPCN2 | OCA2 | SLC45A2 | SLC24A4 | BAP1 | TYRP1

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

Other Diseases

Tetanus | HUPRA Syndrome | Gnathodiaphyseal Dysplasia | Alopecia Totalis | Episodic Ataxia Type 2 | Keratitis | Recurrent Respiratory Papillomatosis | Retinal Vasculitis | Carpenter Syndrome | LRBA Deficiency | Congenital Dyserythropoietic Anemia Type 1 | Congenital Myopathy | Alstrom Syndrome | Autosomal Recessive Spastic Paraplegia Type 35 | Down Syndrome | Glutaric Aciduria Type 1 | Localized Scleroderma | Granular Corneal Dystrophy Type 1 | Aicardi-Goutieres Syndrome | Chorea | Macular Corneal Dystrophy | Atopic Dermatitis | Glycogen Storage Disease Type 0 | Cardiomyopathy, Peripartum | Rotor Syndrome | Pouchitis | Paternal Uniparental Disomy Of Chromosome 14 | Spinocerebellar Ataxia Type 21 | Intestinal Obstruction | Progressive Encephalopathy-optic Atrophy Syndrome | Fontaine Progeroid Syndrome | Tinea | Proopiomelanocortin Deficiency | Dubin-Johnson Syndrome | Cryopyrin-associated Periodic Syndromes | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Schindler Disease | Treacher Collins Syndrome | Hypopituitarism | Cancer, Colon | Alveolar Capillary Dysplasia | Asperger Syndrome | Neurogenic Bladder | Potocki-Shaffer Syndrome | Superficial Spreading Melanoma | Arterial Tortuosity Syndrome | Osteogenesis Imperfecta | Renal-hepatic-pancreatic Dysplasia | Neurofibromatosis-Noonan Syndrome | Hydrocephalus | Blomstrand Osteochondrodysplasia | Juvenile Hyaline Fibromatosis | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Tyrosinemia Type 2 | Membranous Nephropathy | Retinal Dystrophy | Thyroiditis | Panniculitis | Melnick-Needles Syndrome | Neurofibroma | Cenani-Lenz Syndactyly Syndrome | Primary Aldosteronism | Pneumoconiosis | Myotonia | Asthma, Nocturnal | Low Phospholipid Associated Cholelithiasis | Partington Syndrome | Familial Digital Arthropathy-brachydactyly | Myasthenia | Prurigo Nodularis | Familial Exudative Vitreoretinopathy | Coffin-Siris Syndrome | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Hereditary Folate Malabsorption | Anuria | Carcinoma, Merkel Cell | Triple A Syndrome | Congestive Heart Failure | Amyloidosis | Epiphyseal Chondrodysplasia, Miura Type | Pernicious Anemia | Dystonia Musculorum Deformans | Hypertension | Scapuloperoneal Spinal Muscular Atrophy | Empyema | Patent Ductus Arteriosus | Thrombotic Microangiopathy | Cholangitis | Intestinal Hypomagnesemia 1 | IgA Nephropathy | Corneal Neovascularization | Palsy, Cerebral | Waldenstrom Macroglobulinemia | Hemophagocytic Lymphohistiocytosis | Nicotine Addiction | Diastrophic Dysplasia | Erythema Multiforme | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Lichen Planus | Currarino Syndrome | Limb Girdle Muscular Dystrophy | Orotic Aciduria | Congenital Disorders Of Glycosylation | Erysipelas | Cellulitis | Acquired Partial Lipodystrophy | Neuromyotonia | Wiskott-Aldrich Syndrome | Mountain Sickness | Hemangioblastoma | Marshall-Smith Syndrome | Bone Marrow Necrosis | Rhabdomyosarcoma | Emery-Dreifuss Muscular Dystrophy | Dentinogenesis Imperfecta | Hypercalciuria | Acute Kidney Injury | Vogt-Koyanagi-Harada Syndrome | Mitochondrial Encephalomyopathy | Dystrophy, Cone-rod | Primary Hyperoxaluria Type 3 | Bullous Pemphigoid | Angioedema, Acquired | Hyperparathyroidism, Primary | Porphyria, Acute Intermittent | Dystonia | Congenital Sodium Diarrhea | Hyperkeratosis | Osteogenesis Imperfecta Type III | IgA Deficiency | Papilledema | Clouston Hidrotic Ectodermal Dysplasia | Trichotillomania | Carcinoma, Transitional Cell | Spinal Muscular Atrophy Type 3 | Pendred Syndrome | Hypertensive Nephropathy | X-linked Sideroblastic Anemia | Cartilage Disorders | Rash | Otosclerosis | Klinefelter Syndrome | Thrombocytopenia | Hypervalinemia | Microcephaly | Charcot-Marie-Tooth Disease Axonal Type 2N | Hernia, Inguinal | Sturge-Weber Syndrome | Peutz-Jeghers Syndrome | T-cell Prolymphocytic Leukemia | Evans Syndrome | Alagille Syndrome | Wolfram Syndrome | Hereditary Hemorrhagic Telangiectasia | Familial Mediterranean Fever | Lesch-Nyhan Syndrome | Costello Syndrome | Congenital Diaphragmatic Hernia | Astigmatism | Sick Sinus Syndrome | Pulmonary Alveolar Microlithiasis | Pure Autonomic Failure | Liver Failure | Basal Ganglia Disease | Globozoospermia | Meier-Gorlin Syndrome | Holt-Oram Syndrome | Cerebral Amyloid Angiopathy | Gastrointestinal Disorders | Demyelinating Diseases | Pineoblastoma | Familial Cerebral Amyloid Angiopathy | Ovarian Sex Cord-stromal Tumor | Vitreoretinal Degeneration, Snowflake Type | Herpes Genitalis | Papulopustular Rosacea | Filariasis | Sarcosinemia | Cutaneous Lupus Erythematosus | Paraganglioma, Carotid Body | Mycosis Fungoides | Kawasaki Disease | Spinocerebellar Ataxia Type 6 | Periventricular Leukomalacia | Diarrhea | Sarcoma, Alveolar Soft Part | Otitis Media | Metaphyseal Chondrodysplasia, Schmid Type | Mucormycosis | Jacobsen Syndrome | Kidney Stones | VACTERL/VATER Association | Stroke | Alpha-1 Antitrypsin Deficiency | Heterotopic Ossification | Silicosis | Arthropathy | Microcephaly, Seizures, And Developmental Delay | Fragile X Syndrome | Hypertrophy | Hemorrhagic Disorders | Orthostatic Intolerance | Hereditary Sensory Neuropathy Type 1 | Dyggve-Melchior-Clausen Disease | Vici Syndrome | Nail Disorder, Nonsyndromic Congenital | Cerebrotendinous Xanthomatosis | Hypotonia-cystinuria Syndrome | Heroin Dependence | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Persistent Mullerian Duct Syndrome | Temporal Lobe Epilepsy | Hemochromatosis | Retinitis | Rett Syndrome | Presbycusis | Pemphigus | Fundus Albipunctatus | Imerslund-Grasbeck Syndrome | Aplastic Anemia | Histoplasmosis | Neutrophilia | Retinal Diseases | Migraine | Cavitary Optic Disc Anomalies | Atherosclerosis | C3 Glomerulonephritis | Facioscapulohumeral Muscular Dystrophy Type 2 | Stuttering | Cataplexy | Farber Disease | Infantile Liver Failure Syndrome 1 | Encephalocele | Diabetes Type 1 | Congenital Poikiloderma | Neurofibromatosis Type 1 | Endophthalmitis | Hypophosphatasia | Polycythemia Vera | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Eccrine Porocarcinoma | Choroiditis | Congenital Myasthenic Syndrome | Spinocerebellar Ataxia Type 15 | Primary Hyperoxaluria | Chondroma | Frank-ter Haar Syndrome | Persistent Fetal Circulation | Nanophthalmos | Hemangioendothelioma | Sorsby Fundus Dystrophy | Corneal Dystrophies, Hereditary | Hyperlipidemia Type V | Muscular Dystrophy | Discoid Lupus Erythematosus | Tuberculosis | Palmoplantar Keratoderma | Congenital Lipoid Adrenal Hyperplasia | Ichthyosis Hystrix, Curth-Macklin Type | Congenital Hypofibrinogenemia | Carcinoma In Situ | Hypohidrotic Ectodermal Dysplasia | Smith-Lemli-Opitz Syndrome | Purpura | Microtia | Huntington's Disease | Spinocerebellar Ataxia Type 7 | Blepharitis | Hypereosinophilic Syndrome | Beckwith-Wiedemann Syndrome | Pulmonary Capillary Hemangiomatosis | Prostatitis | Niemann-Pick Disease, Type C | Chromosome 17q21.31 Deletion Syndrome | CREST Syndrome | X-linked Myotubular Myopathy | Li-Fraumeni Syndrome | Juvenile Xanthogranuloma | Retinal Telangiectasia | Adenosine Deaminase 2 Deficiency | Hyperprolactinemia | Myoclonus-dystonia Syndrome | Bietti Crystalline Dystrophy | Cleidocranial Dysplasia | Pneumonia, Bacterial | Dermatomyositis | Ornithine Transcarbamylase Deficiency | Keratoconus | Long QT Syndrome Type 1 | Pseudohypoparathyroidism Type 1A | Hypertension, Essential | Non-proliferative Diabetic Retinopathy | Episodic Ataxia Type 1 | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Diabetes Insipidus | Azoospermia | Epilepsy Of Infancy With Migrating Focal Seizures | Fanconi Anemia | Venous Insufficiency | Mast Cell Leukemia | Stiff-man Syndrome | Wolman Disease | Ollier Disease | Lamellar Ichthyosis | Pontocerebellar Hypoplasia | Glucagonoma | Perry Syndrome | Rosacea | Cole-Carpenter Syndrome | Glycogen Storage Disease Type 9 | Osteogenesis Imperfecta Type V | Gout | Gardner Syndrome | Walker-Warburg Syndrome | Oligospermia | Congenital Ichthyosiform Erythroderma | Thrombosis | Oculopharyngeal Muscular Dystrophy | Coma | Arts Syndrome | Riboflavin Transporter Deficiency Neuronopathy | Dysequilibrium Syndrome | Cone Dystrophy | Norrie Disease | Ganglioglioma | Tyrosine Hydroxylase Deficiency | Myocarditis | Strabismus | Heterotaxy | Hypersensitivity Pneumonitis | Short-chain Acyl-CoA Dehydrogenase Deficiency | Colorectal Adenoma | Hyperphenylalaninemia | Vitamin D Deficiency | Chitayat Syndrome | Meconium Ileus | Hyperthyroidism | Blepharo-cheilo-odontic Syndrome | Niemann-Pick Disease | Spinal Muscular Atrophy Type 2 | Cancer, Kidney | Vascular Cognitive Impairment | Thrombophlebitis | Sotos Syndrome | WAGR Syndrome | Leukodystrophies | Leiomyoma | Parkinson Disease 6, Autosomal Recessive Early-onset | Pantothenate Kinase-associated Neurodegeneration | Oculocutaneous Albinism | Growth Hormone Excess | Cold-induced Sweating Syndrome | Olmsted Syndrome | Schistosomiasis | Alpers Syndrome | Familial Hemiplegic Migraine | Cutaneous Mastocytosis | Supravalvular Aortic Stenosis | Antisynthetase Syndrome | Bipolar Disorder | Lathosterolosis | Hypermethioninemia | Porencephaly | Tay-Sachs Disease | Aromatic L-amino Acid Decarboxylase Deficiency | Erectile Dysfunction | Jaundice, Obstructive | Familial Hypobetalipoproteinemia | Spondylo-ocular Syndrome | Tyrosinemia | Hepatitis C, Chronic | Paronychia | Psoriasis | Fowler's Syndrome | Retinoschisis | Glioma | Combined Malonic And Methylmalonic Acidemia | Myelodysplasia | Onchocerciasis | Intestinal Pseudo-obstruction | Chromosome 8q21.11 Deletion Syndrome | Hypercholesterolemia, Familial | Postpoliomyelitis Syndrome | Jalili Syndrome | Neuromuscular Disorders | Thanatophoric Dysplasia | Hepatitis | Micropenis | Leprosy | Malaria | Hamartoma | Amyotrophic Lateral Sclerosis | Osmotic Demyelination Syndrome | Chronic Granulomatous Disease, X-linked | Synpolydactyly | Mucolipidosis Type III | Crimean-Congo Hemorrhagic Fever | Meningitis | Noonan Syndrome | Irritable Bowel Syndrome