Associated diseases in tRF-Tyr-GTA-011

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.
Carcinoma, Renal CellDOID:4467clear cell renal cell carcinomadisease of anatomical entity//disease of cellular proliferationA renal cell carcinoma that has_material_basis_in cells that appear very pale or clear when examined under microscope.
CardiomegalyN/AN/AN/AN/A
Cardiomyopathy, DilatedDOID:12930 dilated cardiomyopathydisease of anatomical entityAn intrinsic cardiomyopathy that is characterized by an an enlarged heart and damage to the myocardium causing the heart to pump blood inefficiently.
Cardiomyopathy, HypertrophicDOID:11984hypertrophic cardiomyopathydisease of anatomical entityAn intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause.
Cartilage DiseasesDOID:1222 cartilage diseasedisease of anatomical entityA connective tissue disease that is located_in cartilage.
Fetal Growth RetardationN/AN/AN/AN/A
Fibrous Dysplasia of BoneDOID:0080031fibrous dysplasiadisease of anatomical entity A bone remodeling disease that results_in the destruction of normal bone and replacing it with fibrous bone tissue.
Graves OphthalmopathyDOID:0081120Graves ophthalmopathydisease of anatomical entityAn autoimmune disease of eyes, ear, nose and throat that is characterized by upper eyelid retraction, lid lag, swelling, redness, conjunctivitis, and bulging eyes.
Heart Defects, CongenitalDOID:1682congenital heart diseasephysical disorder//disease of anatomical entityN/A
Heart FailureN/AN/AN/AN/A
KeloidN/AN/AN/AN/A
Kidney DiseasesDOID:557kidney diseasedisease of anatomical entityA urinary system disease that is located_in the kidney.
Lupus Erythematosus, SystemicDOID:9074systemic lupus erythematosusdisease of anatomical entityA lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart.
Mycoplasma InfectionsN/AN/AN/AN/A
Myocardial IschemiaN/AN/AN/AN/A
MyocarditisDOID:820myocarditisdisease of anatomical entityAn extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle.
Nephrotic SyndromeN/AN/AN/AN/A
Oral Submucous FibrosisDOID:5773oral submucous fibrosisdisease of anatomical entityA mouth disease that is characterized by juxta-epithelial inflammatory reaction and progressive fibrosis of the submucosal tissues.
OsteoarthritisDOID:8398osteoarthritisdisease of anatomical entityAn arthritis that has_material_basis_in worn out cartilage located_in joint.
Polycystic Ovary SyndromeDOID:11612polycystic ovary syndromedisease of anatomical entity//reproductive system diseaseAn ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight.
Rheumatic Heart DiseaseDOID:0050827rheumatic heart diseasedisease of anatomical entityA heart valve disease that is characterized by repeated inflammation with fibrinous repair caused by an autoimmune reaction to Group A beta-hemolytic streptococci (GAS) that results in valvular damage. The cardinal anatomic changes of the valve include leaflet thickening, commissural fusion, and shortening and thickening of the tendinous cords.
Spotted Fever Group RickettsiosisDOID:11103rickettsialpoxdisease by infectious agentA spotted fever that has_material_basis_in Rickettsia akari, which is transmitted_by house mouse mite (Liponyssoides sanguineus) found on mice and other rodents. The infection has_symptom fever, has_symptom chills, has_symptom headache, has_symptom myalgia, and has_symptom papulovesicular rash.