Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0020538 Hypertensive disease group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 284
C0023893 Liver Cirrhosis, Experimental disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Experimental Model of Disease 125
C0149940 Sciatic Neuropathy disease Nervous System Diseases Disease or Syndrome disease of anatomical entity 109
C0740392 Infarction, Middle Cerebral Artery disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 108
C0014072 Experimental Autoimmune Encephalomyelitis disease Immune System Diseases; Nervous System Diseases Experimental Model of Disease 89
C0038454 Cerebrovascular accident group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the nervous system; Abnormality of the cardiovascular system 64
C0034069 Pulmonary Fibrosis disease Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity Abnormality of the respiratory system 47
C0242706 Hyperoxia phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 42
C2936380 Neointima disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 33
C0403592 Chronic rejection of renal transplant disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 7
C0079924 Oligohydramnios phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function disease of anatomical entity Abnormality of prenatal development or birth 5
C0157738 Chronic skin ulcer disease Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity 2