CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0010054 Coronary Arteriosclerosis disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 65 0
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 62 198
C0751956 Acute Cerebrovascular Accidents disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 54 0
C0020443 Hypercholesterolemia disease Nutritional and Metabolic Diseases Disease or Syndrome Abnormality of metabolism/homeostasis 39 10
C0700292 Hypoxemia phenotype Pathological Conditions, Signs and Symptoms Finding Abnormality of the respiratory system 33 7
C0003129 Anoxemia phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 33 0
C0003130 Anoxia phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 33 0
C0242184 Hypoxia phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 33 0
C0013604 Edema phenotype Pathological Conditions, Signs and Symptoms Pathologic Function Abnormality of metabolism/homeostasis 26 1
C0151603 Anasarca phenotype Pathological Conditions, Signs and Symptoms Pathologic Function Abnormality of metabolism/homeostasis 26 0
C0004943 Behcet Syndrome disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 24 52
C0268731 Renal glomerular disease group Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system 23 1
C0011609 Drug Eruptions group Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders Disease or Syndrome 23 0
C0406537 Morbilliform Drug Reaction disease Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders Disease or Syndrome 23 0
C4521256 Glomerulopathy Assessment phenotype Diagnostic Procedure 23 0
C0242488 Acute Lung Injury disease Respiratory Tract Diseases Injury or Poisoning 22 3
C0853897 Diabetic Cardiomyopathies disease Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0
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 6 23
C0086445 Idiopathic Membranous Glomerulonephritis disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 6 0
C1704378 Heymann Nephritis disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 6 0
C0268389 Amyloidosis, familial visceral disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome disease of metabolism 5 15
C2362324 Pediatric Obesity disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 4 0
C4317171 Adolescent Obesity phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 4 0
C4521075 Childhood Overweight phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Finding 4 0
C4553478 Infantile Obesity phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 4 0