Source: CURATED

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C4277682 Chemical and Drug Induced Liver Injury disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404 38
C0860207 Drug-Induced Liver Disease phenotype Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404 1
C0019193 Hepatitis, Toxic disease Digestive System Diseases; Chemically-Induced Disorders Injury or Poisoning 404 0
C1262760 Hepatitis, Drug-Induced disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404 0
C3658290 Drug-Induced Acute Liver Injury disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404 0
C4279912 Chemically-Induced Liver Toxicity disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404 0
C0011860 Diabetes Mellitus, Non-Insulin-Dependent disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome disease of metabolism Abnormality of metabolism/homeostasis; Abnormality of the endocrine system 221 1232
C2609414 Acute kidney injury disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Injury or Poisoning disease of anatomical entity Abnormality of the genitourinary system 101 3
C0022660 Kidney Failure, Acute disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome Abnormality of the genitourinary system 101 0
C1565662 Acute Kidney Insufficiency disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity 101 0
C0013221 Drug toxicity group Chemically-Induced Disorders Injury or Poisoning 84 0
C0041755 Adverse reaction to drug group Chemically-Induced Disorders Pathologic Function 84 0
C0021655 Insulin Resistance phenotype Nutritional and Metabolic Diseases Pathologic Function Abnormality of metabolism/homeostasis 60 53
C0920563 Insulin Sensitivity phenotype Nutritional and Metabolic Diseases Pathologic Function 60 0
C0238281 Middle Cerebral Artery Syndrome phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34 0
C0740376 Middle Cerebral Artery Thrombosis disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34 0
C0740391 Middle Cerebral Artery Occlusion disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 34 0
C0740392 Infarction, Middle Cerebral Artery disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 34 0
C0751845 Middle Cerebral Artery Embolus phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34 0
C0751846 Left Middle Cerebral Artery Infarction phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34 0
C0751847 Embolic Infarction, Middle Cerebral Artery phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34 0
C0751848 Thrombotic Infarction, Middle Cerebral Artery phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34 0
C0751849 Right Middle Cerebral Artery Infarction phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34 0
C0272242 Complement deficiency disease group Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome disease of anatomical entity Abnormality of the immune system 33 0
C0242383 Age related macular degeneration disease Eye Diseases Disease or Syndrome genetic disease; disease of anatomical entity 30 349