Source: CTD_human

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0018801 Heart failure disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 110
C0018802 Congestive heart failure disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 110
C0023212 Left-Sided Heart Failure disease Cardiovascular Diseases Disease or Syndrome Abnormality of the cardiovascular system 110
C0235527 Heart Failure, Right-Sided disease Cardiovascular Diseases Disease or Syndrome Abnormality of the cardiovascular system 110
C1959583 Myocardial Failure disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 110
C1961112 Heart Decompensation phenotype Cardiovascular Diseases Pathologic Function 110
C0028043 Nicotine Dependence disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction disease of mental health 14
C0040332 Tobacco Dependence disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 14
C0376384 Nicotine Use Disorder phenotype Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 14
C0019202 Hepatolenticular Degeneration disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome genetic disease; disease of metabolism; disease of anatomical entity 24
C1527352 Hepatic Form of Wilson Disease disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 24
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 16
C0013080 Down Syndrome disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome genetic disease 19
C0432416 Down Syndrome, Partial Trisomy 21 disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 19
C0432417 Trisomy 21, Meiotic Nondisjunction disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 19
C0751081 Trisomy 21, Mitotic Nondisjunction disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 19
C0008370 Cholestasis disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 99
C0015695 Fatty Liver disease Digestive System Diseases Disease or Syndrome genetic disease; disease of metabolism 88
C2711227 Steatohepatitis disease Digestive System Diseases Disease or Syndrome Abnormality of the digestive system 88
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 60
C0017168 Gastroesophageal reflux disease disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 4
C0014869 Peptic Esophagitis disease Digestive System Diseases Disease or Syndrome disease of anatomical entity 1
C0019187 Hepatitis, Alcoholic disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome disease of anatomical entity 5
C0524610 Chronic Alcoholic Hepatitis disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 5
C2239176 Liver carcinoma disease Digestive System Diseases; Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation Abnormality of the digestive system; Neoplasm 501