Associated diseases in tRF-22-WE8SPOX52


DiseaseDO_IDDO_NameDO_TypeDO_Define
Atrial FibrillationDOID:0060224atrial fibrillationdisease of anatomical entityA heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain.
Colorectal NeoplasmsDOID:9256colorectal cancerdisease of anatomical entity//disease of cellular proliferationA large intestine cancer that is located_in the colon and/or located_in the rectum.
Diffuse Intrinsic Pontine GliomaDOID:0080880diffuse glioma, H3 G34 mutantdisease of cellular proliferationA histone mutated tumor that has_material_basis_in mutations in codon 34 of the H3 histone family 3A protein.
Leukemia, Lymphocytic, Chronic, B-CellDOID:1040chronic lymphocytic leukemiadisease of anatomical entity//disease of cellular proliferationA lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood.
Multiple MyelomaDOID:9538multiple myelomadisease of anatomical entity//disease of cellular proliferationA myeloid neoplasm that is located_in the plasma cells in bone marrow.
Reperfusion InjuryN/AN/AN/AN/A
StrokeN/AN/AN/AN/A