Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0178664 Glomerulosclerosis (disorder) disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome Abnormality of the genitourinary system 14
C0085548 Autosomal Recessive Polycystic Kidney Disease disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome genetic disease; disease of anatomical entity 13
C0025261 Memory Disorders disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 10
C0520679 Sleep Apnea, Obstructive disease Respiratory Tract Diseases; Nervous System Diseases Disease or Syndrome disease of mental health Abnormality of the nervous system; Abnormality of the respiratory system 9
C0006272 Bronchiolitis Obliterans disease Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity Abnormality of the respiratory system 8
C0521607 Peritoneal Fibrosis disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 8
C0042510 Ventricular Fibrillation disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome Abnormality of the cardiovascular system 5
C0005586 Bipolar Disorder disease Mental Disorders Mental or Behavioral Dysfunction disease of mental health Abnormality of the nervous system 3
C0005587 Depression, Bipolar disease Mental Disorders Mental or Behavioral Dysfunction disease of mental health 3
C0024713 Manic Disorder disease Mental Disorders Mental or Behavioral Dysfunction disease of mental health 3
C0236780 Mixed bipolar I disorder disease Mental Disorders Mental or Behavioral Dysfunction disease of mental health 3
C4054127 Radiation Nephropathy disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 2
C0003492 Aortic coarctation disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality Abnormality of the cardiovascular system 1
C0009714 Hepatic Fibrosis, Congenital disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of the digestive system 1
C0028841 Ocular Hypotension disease Eye Diseases Disease or Syndrome disease of anatomical entity 1
C0264657 Renal sclerosis with hypertension disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 1
C0282548 Leukostasis disease Hemic and Lymphatic Diseases Disease or Syndrome disease of anatomical entity 1
C0451720 Nephrotic syndrome, focal and segmental glomerular lesions disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome genetic disease; disease of anatomical entity 1
C2902887 Nephrotic syndrome with focal and segmental hyalinosis disease Disease or Syndrome genetic disease; disease of anatomical entity 1
C2902888 Nephrotic syndrome with focal and segmental sclerosis disease Disease or Syndrome genetic disease; disease of anatomical entity 1
C2902889 Nephrotic syndrome with focal glomerulonephritis disease Disease or Syndrome genetic disease; disease of anatomical entity 1
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
C0376618 Endotoxemia phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 101
C0018800 Cardiomegaly phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Finding Abnormality of the cardiovascular system 95
C0015934 Fetal Growth Retardation phenotype Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome Growth abnormality 71