Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C4721773 Postoperative cognitive dysfunction phenotype Mental or Behavioral Dysfunction 3
C4553639 Arterial Injury, CTCAE phenotype Finding 4
C4552089 HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME disease Disease or Syndrome genetic disease; disease of metabolism 3
C4551527 Focal segmental glomerulosclerosis 1 disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome genetic disease; disease of anatomical entity 1
C4551463 Colon adenoma disease Digestive System Diseases; Neoplasms Neoplastic Process 1
C4540036 FRASER SYNDROME 2 disease Disease or Syndrome genetic disease 1
C4277682 Chemical and Drug Induced Liver Injury disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 44
C4054127 Radiation Nephropathy disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 2
C4048195 Autosomal dominant hypocalcemia disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome genetic disease; disease of metabolism 3
C3887915 AERODIGESTIVE TRACT CANCER, SQUAMOUS CELL, ALCOHOL-RELATED, PROTECTION AGAINST phenotype Finding disease of mental health 2
C3887892 Aortic Valve Disease 1 disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 1
C3850141 Acute-On-Chronic Liver Failure disease Digestive System Diseases Disease or Syndrome 2
C3825727 Respiratory allergy phenotype Pathologic Function 1
C3809278 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET disease Disease or Syndrome disease of anatomical entity 1
C3805040 Phospholipidosis disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 1
C3715128 HYPOCALCEMIA, AUTOSOMAL DOMINANT 1 disease Disease or Syndrome genetic disease; disease of metabolism 3
C3714630 Respirovirus Infections disease Infections Disease or Syndrome 1
C3714509 Nutrition Disorders group Nutritional and Metabolic Diseases Disease or Syndrome disease of metabolism 1
C3711385 Deoxyguanosine Kinase Deficiency disease Nutritional and Metabolic Diseases Disease or Syndrome genetic disease; disease of metabolism 1
C3665444 Neutrophilia (disorder) disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 1
C3665419 intracranial glioma disease Neoplasms; Nervous System Diseases Neoplastic Process 7
C3658208 Dysbiosis phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 1
C3495676 Anorectal Malformations group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Anatomical Abnormality disease of anatomical entity Abnormality of the digestive system 6
C3489856 Cold Hypersensitivity disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 1
C3278923 Dilated ventricles (finding) phenotype Finding Abnormality of the nervous system 1