Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0038358 Gastric ulcer disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 33
C0017638 Glioma disease Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation Abnormality of the nervous system; Neoplasm 33
C0023890 Liver Cirrhosis disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 33
C0555198 Malignant Glioma disease Neoplasms Neoplastic Process disease of cellular proliferation 33
C2936380 Neointima disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 33
C0024117 Chronic Obstructive Airway Disease disease Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity Abnormality of the respiratory system 32
C0011854 Diabetes Mellitus, Insulin-Dependent disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome genetic disease; disease of metabolism Abnormality of metabolism/homeostasis; Abnormality of the endocrine system 32
C0027814 Neuritis, Autoimmune, Experimental disease Immune System Diseases; Nervous System Diseases Experimental Model of Disease 32
C0267941 Pancreatitis, Acute Necrotizing disease Digestive System Diseases Disease or Syndrome 32
C0162770 Right Ventricular Hypertrophy disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome Abnormality of the cardiovascular system 32
C0020456 Hyperglycemia disease Nutritional and Metabolic Diseases Disease or Syndrome disease of metabolism Abnormality of metabolism/homeostasis 30
C0020550 Hyperthyroidism disease Endocrine System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the endocrine system 30
C0022116 Ischemia phenotype Pathological Conditions, Signs and Symptoms Pathologic Function disease of anatomical entity 30
C0042164 Uveitis disease Eye Diseases Disease or Syndrome disease of anatomical entity Abnormality of the immune system; Abnormality of the eye 30
C0027726 Nephrotic Syndrome group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of the genitourinary system 29
C0014544 Epilepsy disease Nervous System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the nervous system 28
C0017601 Glaucoma disease Eye Diseases Disease or Syndrome disease of anatomical entity Abnormality of the eye 28
C0020476 Hyperlipoproteinemias disease Nutritional and Metabolic Diseases Disease or Syndrome genetic disease; disease of metabolism Abnormality of metabolism/homeostasis 28
C0026846 Muscular Atrophy phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Pathologic Function disease of anatomical entity 28
C0027720 Nephrosis disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity 28
C0023892 Biliary cirrhosis disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 27
C0011882 Diabetic Neuropathies group Nervous System Diseases; Endocrine System Diseases Disease or Syndrome disease of anatomical entity 27
C0020473 Hyperlipidemia disease Nutritional and Metabolic Diseases Disease or Syndrome genetic disease; disease of metabolism Abnormality of metabolism/homeostasis 27
C0008312 Primary biliary cirrhosis disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 27
C0242184 Hypoxia phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 26