| exon_id | ENSE00001345243, ENSE00003653682, ENSE00003530156, ENSE00003523148, ENSE00003615787, ENSE00003537296, ENSE00003629136, ENSE00001167794, ENSE00001167801, ENSE00001167809, ENSE00001167814, ENSE000011678 |
| disease_description | FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder),Meckel syndrome type 1,Congenital Abnormality,Fanconi Anemia,Cancer of Head and Neck,Malignant neoplasm of thyroid,Hemimegalencephaly,Liver and Intrahepatic Biliary Tract Carcinoma,Pituitary Neoplasms,T-Cell Lymphoma,Angiofibroma,Congenital chromosomal disease,Adenocarcinoma Of Esophagus,Precursor T-Cell Lymphoblastic Leukemia-Lymphoma,Lupus Erythematosus, Systemic,HIV Infections,Mastocytosis, Systemic,Advanced cancer,Thymus Hyperplasia,Metastatic malignant neoplasm to brain,Malonic aciduria,Fetal Growth Retardation,Benign Neoplasm,Nasal Polyps,Lupus Erythematosus, Discoid,FRAGILE X TREMOR/ATAXIA SYNDROME,Chronic Kidney Insufficiency,Primary Myelofibrosis,Myeloid Leukemia, Chronic,Kaposiform Hemangioendothelioma,Gestational Diabetes,Pre B-cell acute lymphoblastic leukemia,Endometrial Carcinoma,Malignant neoplasm of kidney,Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse,Osteosarcoma of bone,Myocardial Infarction,M |