Source: CTD_human

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0004238 Atrial Fibrillation disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 156
C3468561 familial atrial fibrillation phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 156
C0235480 Paroxysmal atrial fibrillation disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome Abnormality of the cardiovascular system 156
C2585653 Persistent atrial fibrillation phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 156
C0751956 Acute Cerebrovascular Accidents disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 54
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 54
C0003811 Cardiac Arrhythmia phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome Abnormality of the cardiovascular system 19
C0003123 Anorexia disease Pathological Conditions, Signs and Symptoms Disease or Syndrome Abnormality of the digestive system 18
C0080203 Tachyarrhythmia phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Finding 18
C0039231 Tachycardia phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Finding Abnormality of the cardiovascular system 18
C0001627 Congenital adrenal hyperplasia disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome genetic disease; disease of metabolism Abnormality of the endocrine system 9