Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0334096 Intimal proliferation phenotype Pathologic Function 7
C0007194 Hypertrophic Cardiomyopathy disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 11
C0025427 Mercury Poisoning disease Chemically-Induced Disorders Injury or Poisoning 2
C0949658 Cardiomyopathy, Hypertrophic, Familial disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 11
C0035344 Retinopathy of Prematurity disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of the eye 10
C0598608 Hyperhomocysteinemia disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome genetic disease; disease of metabolism 22
C0020192 Hyaline Membrane Disease disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity 5
C0009319 Colitis disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system; Abnormality of the immune system 51
C0030305 Pancreatitis disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system; Abnormality of the immune system 41
C0267941 Pancreatitis, Acute Necrotizing disease Digestive System Diseases Disease or Syndrome 32
C0009324 Ulcerative Colitis disease Digestive System Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of the digestive system; Abnormality of the immune system 12
C0375359 Chronic left-sided ulcerative colitis disease Digestive System Diseases Disease or Syndrome disease of anatomical entity 12
C0014335 Enteritis disease Digestive System Diseases Disease or Syndrome disease of anatomical entity 3
C0025472 Mesenteric Vascular Occlusion disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 1
C0160390 Injury of liver disease Digestive System Diseases; Wounds and Injuries Injury or Poisoning 36
C0011875 Diabetic Angiopathies disease Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 9
C0042164 Uveitis disease Eye Diseases Disease or Syndrome disease of anatomical entity Abnormality of the immune system; Abnormality of the eye 30
C0011884 Diabetic Retinopathy disease Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 42
C0032914 Pre-Eclampsia phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function disease of anatomical entity Abnormality of prenatal development or birth 14
C0022661 Kidney Failure, Chronic disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity 85
C2609414 Acute kidney injury disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Injury or Poisoning disease of anatomical entity Abnormality of the genitourinary system 80
C2316810 Chronic kidney disease stage 5 disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome Abnormality of the genitourinary system 58
C0029866 Other ureteric obstruction phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Anatomical Abnormality disease of anatomical entity 52
C0027697 Nephritis disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system; Abnormality of the immune system 18
C0011881 Diabetic Nephropathy disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 120