exon_id | ENSE00003790474, ENSE00003674725, ENSE00003620454, ENSE00003685219, ENSE00003192504, ENSE00003145022, ENSE00003173612, ENSE00003042006, ENSE00003175276, ENSE00003187600 |
disease_description | Congenital Abnormality,Amyloid Neuropathies, Familial,Colonic Polyps,Diarrhea,Hereditary Nonpolyposis Colorectal Cancer,Fibromatosis, Aggressive,Vascular Diseases,Chronic Lymphocytic Leukemia,Adenocarcinoma,Retinoblastoma,HIV Infections,Plaque, Amyloid,Polyneuropathy,Hamartoma,Adenoma,Lupus Nephritis,Stromal Neoplasm,Gardner fibroma,Carpal Tunnel Syndrome,Congenital abnormality of vein,MUTYH-Associate Polyposis,Ulnar Nerve Entrapment Syndrome,Hereditary Breast and Ovarian Cancer Syndrome,Ovarian Carcinoma,Severe diarrhea,Congenital hypertrophy,polyps,Liver carcinoma,Malignant tumor of colon,Neuropathy,AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED,Carcinogenesis,Adenocarcinoma of duodenum,Actinic keratosis,Colorectal Cancer,Multiple polyps,Colorectal Carcinoma,Familial Amyloid Neuropathy, Portuguese Type,Polyp of large intestine,psychological distress,Amyloidosis,HIV-Associated Lipodystrophy Syndrome,Graft-vs-Host Disease,Familial Amyloid Polyneuropathy, Type IV,Adenomatous Polyposis C |