Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0026846 Muscular Atrophy phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Pathologic Function disease of anatomical entity 28
C0151650 Renal fibrosis disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome Abnormality of the genitourinary system 21
C1397307 Cardiac fibrosis disease Disease or Syndrome 17
C0162871 Aortic Aneurysm, Abdominal disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 16
C0011849 Diabetes Mellitus group Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome disease of metabolism Abnormality of metabolism/homeostasis; Abnormality of the endocrine system 16
C0042487 Venous Thrombosis phenotype Cardiovascular Diseases Pathologic Function disease of anatomical entity Abnormality of blood and blood-forming tissues 15
C0017668 Focal glomerulosclerosis disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system 14
C0178664 Glomerulosclerosis (disorder) disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome Abnormality of the genitourinary system 14
C0007785 Cerebral Infarction disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 12
C0026766 Multiple Organ Failure phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 11
C0019080 Hemorrhage phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 10
C0012739 Disseminated Intravascular Coagulation disease Hemic and Lymphatic Diseases Disease or Syndrome disease of anatomical entity Abnormality of blood and blood-forming tissues 7
C0151942 Arterial thrombosis phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function Abnormality of blood and blood-forming tissues 4
C0003486 Aortic Aneurysm disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 2
C0741160 Aortic Aneurysm, Ruptured disease Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome disease of anatomical entity 2
C0156181 Peritoneal adhesion disease Digestive System Diseases; Skin and Connective Tissue Diseases Acquired Abnormality 2
C0375362 Peritoneal adhesions (postoperative) (postinfection) disease Disease or Syndrome 2
C4054127 Radiation Nephropathy disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 2
C0265012 Ruptured abdominal aortic aneurysm disease Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome disease of anatomical entity 2
C0265010 Ruptured thoracic aortic aneurysm disease Respiratory Tract Diseases; Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome disease of anatomical entity 2
C1305122 Thoracoabdominal aortic aneurysm, ruptured disease Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome disease of anatomical entity 2
C0018939 Hematological Disease group Hemic and Lymphatic Diseases Disease or Syndrome disease of anatomical entity Abnormality of blood and blood-forming tissues 1
C0032461 Polycythemia disease Hemic and Lymphatic Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of blood and blood-forming tissues 1