Source: CTD_human

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
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
C0027055 Myocardial Reperfusion Injury phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 85
C0458247 Allodynia phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding Constitutional symptom 84
C0020429 Hyperalgesia phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom Abnormality of the nervous system 84
C0751211 Hyperalgesia, Primary phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 84
C0751212 Hyperalgesia, Secondary phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 84
C0751214 Hyperalgesia, Thermal phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 84
C2936719 Mechanical Allodynia phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 84
C0751213 Tactile Allodynia phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 84
C4721507 Alveolitis, Fibrosing disease Respiratory Tract Diseases Disease or Syndrome 83
C0034069 Pulmonary Fibrosis disease Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity Abnormality of the respiratory system 83
C0004096 Asthma disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the immune system; Abnormality of the respiratory system 80
C0023895 Liver diseases group Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 71
C0086565 Liver Dysfunction phenotype Digestive System Diseases Finding Abnormality of the digestive system 71
C0393734 Complex Partial Status Epilepticus disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 67
C0311335 Grand Mal Status Epilepticus disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome disease of anatomical entity 67
C0751523 Non-Convulsive Status Epilepticus disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome Abnormality of the nervous system 67
C0270823 Petit mal status disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 67
C0751524 Simple Partial Status Epilepticus phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 67
C0038220 Status Epilepticus disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the nervous system 67
C0751522 Status Epilepticus, Subclinical disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 67
C0010054 Coronary Arteriosclerosis disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 65
C1956346 Coronary Artery Disease disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 65
C1527304 Allergic Reaction phenotype Immune System Diseases Pathologic Function disease of anatomical entity 63