2875
|
|
|
Melanocyte inducing transcription factor |
CMM8, COMMAD, MI, MITF-A, WS2, WS2A, bHLHe32 |
Curated: Isolated sensorineural deafness, Renal cell carcinoma, Cataract, Chagas cardiomyopathy, Clear cell papillary renal cell carcinoma, Commissural facial cleft, Congenital ear anomaly, Congenital sensorineural hearing loss, Coronary artery disease, Melanoma, Deafness, Dyslexia, Gout, Hearing loss, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Kleins syndrome, Myocardial infarction, Oculocutaneous albinism, Scoliosis, Skin cancer, Skin neoplasms, Tietz syndrome, Diabetes mellitus type 2, Waardenburg syndrome, Waardenburg-shah syndrome, Waardenburg syndrome type 2
Unreviewed: Adrenal Gland Pheochromocytoma, Albinism, Alport Syndrome, Anaplasia, Angiomatoid fibrous histiocytoma, Angiomyolipoma Of Kidney, Anomalous Pulmonary Artery, Atrophy, Attention Deficit Hyperactivity Disorder, Atypical Mole Melanoma Syndrome, B-Cell Lymphoma, Biliary tract neoplasms, Bone disease, Bone resorption, Breast neoplasm, Carcinogenesis, Cholangiocarcinoma, Chondroblastoma, Chromophobe Carcinoma, Classical Hodgkin lymphoma, Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness, Colorectal neoplasm, Congenital ocular coloboma, Congenital Sensorineural Hearing Loss, Congestive Heart Failure, CREST Syndrome, Cutaneous malignant melanoma, Dermatologic Disorders, Diabetes, Diabetes Mellitus, Diabetic foot, Epithelial ovarian carcinoma, Esophageal neoplasm, Esophageal squamous cell carcinoma, Eye abnormalities, Fibromatosis, Frontal bossing, Gastrointestinal stromal tumor, Giant cell tumor of bone, Glioma, Hearing Loss, Heart Failure, Hemangiosarcoma, Hepatocellular carcinoma, Hereditary Cancer Syndrome, Hereditary cutaneous melanoma, Hereditary Paraganglioma-Pheochromocytoma Syndromes, Hirschsprung Disease, Histiocytoma, Hodgkin Disease, Hyperglycemia, Hyperlipoproteinemia, Hyperopia, Hypopigmentation Disorder, Hypoxia, Ichthyosis, Incontinentia Pigmenti Achromians, Intestinal Obstruction, Kidney Cancer, Kidney Disease, Kidney Neoplasm, Leber congenital amaurosis, Leukemia, Liver carcinoma, Lymphatic metastasis, Macrocephaly, Malignant Histiocytoma, Malignant Neoplasm, Malnutrition, Mammary Neoplasms, Mast cell leukemia, Mastocytosis, Medullary carcinoma, Melanocytic nevus, Melasma, Mental retardation, Mesothelioma, Metastatic Melanoma, Micrognathism, Microphthalmos, Monocytic Leukemia, Mouth neoplasm, Multicystic renal dysplasia, Multiple lentigines, Multiple myeloma, Myocardial Infarction, Neoplasms, Nervous System Disorder, Neural Crest Tumor, Neurodegenerative disorder, Nevus, Nodular Fasciitis, Nonsyndromic Deafness, Nystagmus, Ocular albinism, Ocular Albinism With Congenital Sensorineural Deafness, Ocular Albinism With Sensorineural Deafness, Osteopetrosis, Osteoporosis, Ovarian neoplasm, Oxyphilic Adenoma, Pancreatic cancer, Pancreatic carcinoma, Pancreatic Neoplasm, Papillary Renal Carcinoma, Papillary thyroid cancer, Paraganglioma, Parkinson disease, Peritonitis, Perivascular Epithelioid Neoplasms, Pheochromocytoma, Piebaldism, Pigmentation Disorders, Poliosis, Posteriorly Rotated Ear, Prolactinoma, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Ptosis, Renal Carcinoma, Renal Glomerular Disease, Retinal Diseases, Rheumatoid arthritis, Sarcoidosis, Sarcoma, Sensorineural hearing loss, Skin neoplasm, Speech Disorders, Squamous cell carcinoma, Steroid Sulfatase Deficiency Disease, Stomach Carcinoma, Stomach Neoplasms, Strabismus, Syndromic microphthalmia, Synophrys, Tietz Syndrome, Tuberous sclerosis complex, Tumor, Tyrosinase-negative oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism, Uveal melanoma, Vitiligo, Vitiligo-associated SYSTEMIC LUPUS ERYTHEMATOSUS, Von Hippel-Lindau Syndrome
|