exon_id | ENSE00003480655, ENSE00003570149, ENSE00003536582, ENSE00003461069, ENSE00003686077, ENSE00003651039, ENSE00003463524, ENSE00003550537, ENSE00003551369, ENSE00003675027, ENSE00003512497, ENSE000035196 |
disease_description | Hereditary hemochromatosis,Juvenile hemochromatosis,HEMOCHROMATOSIS, TYPE 3,Beta thalassemia intermedia,Precursor Cell Lymphoblastic Leukemia Lymphoma,Prostate carcinoma,Iron deficiency anemia,Liver diseases,Fibrosis, Liver,Acute Erythroblastic Leukemia,Acute leukemia,Hyperplasia erythroid,Malignant neoplasm of breast,Iron Metabolism Disorders,Neonatal hemochromatosis,Malignant neoplasm of prostate,Porphyria Cutanea Tarda,Myeloid Leukemia, Chronic,Hemochromatosis,Hepatitis C, Chronic,Acute lymphocytic leukemia,Cystic Fibrosis,Liver Cirrhosis,Hematocrit level,Age related macular degeneration,Anemia,HFE-Associated Hereditary Hemochromatosis,Liver carcinoma,Rheumatoid Arthritis,leukemia,Leukemia, Myelocytic, Acute,Iron deficiency,Spontaneous abortion,beta Thalassemia,Preleukemia,Hypertensive disease,Astrocytoma,Iron-Refractory Iron Deficiency Anemia,Iron Overload,Liver neoplasms,MYELODYSPLASTIC SYNDROME |