Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0242706 Hyperoxia phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 42
C0038525 Subarachnoid Hemorrhage disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome Abnormality of the nervous system; Abnormality of blood and blood-forming tissues; Abnormality of the cardiovascular system 40
C0024115 Lung diseases group Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity Abnormality of the respiratory system 38
C0160390 Injury of liver disease Digestive System Diseases; Wounds and Injuries Injury or Poisoning 36
C0038358 Gastric ulcer disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 33
C2936380 Neointima disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 33
C0024117 Chronic Obstructive Airway Disease disease Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity Abnormality of the respiratory system 32
C0027814 Neuritis, Autoimmune, Experimental disease Immune System Diseases; Nervous System Diseases Experimental Model of Disease 32
C0162770 Right Ventricular Hypertrophy disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome Abnormality of the cardiovascular system 32
C0020456 Hyperglycemia disease Nutritional and Metabolic Diseases Disease or Syndrome disease of metabolism Abnormality of metabolism/homeostasis 30
C0023892 Biliary cirrhosis disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 27
C0008312 Primary biliary cirrhosis disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 27
C0016059 Fibrosis phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 25
C0020179 Huntington Disease disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders Disease or Syndrome disease of anatomical entity 25
C0022658 Kidney Diseases group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system 24
C0014175 Endometriosis disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system 23
C0027627 Neoplasm Metastasis phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 23
C0017665 Membranous glomerulonephritis disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system; Abnormality of the immune system 22
C0023896 Alcoholic Liver Diseases group Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 21
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
C1527311 Brain Edema phenotype Nervous System Diseases Pathologic Function disease of anatomical entity Abnormality of metabolism/homeostasis; Abnormality of the nervous system 20
C0003850 Arteriosclerosis disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 17
C1397307 Cardiac fibrosis disease Disease or Syndrome 17
C0028840 Ocular Hypertension disease Eye Diseases Disease or Syndrome disease of anatomical entity 17
C0162871 Aortic Aneurysm, Abdominal disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 16