Source: LHGDN

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0040053 Thrombosis phenotype Cardiovascular Diseases Pathologic Function disease of anatomical entity 66
C0243026 Sepsis disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome disease by infectious agent 65
C0025500 Mesothelioma disease Neoplasms Neoplastic Process disease of cellular proliferation 59
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 55
C0948089 Acute Coronary Syndrome disease Cardiovascular Diseases Disease or Syndrome 52
C0022116 Ischemia phenotype Pathological Conditions, Signs and Symptoms Pathologic Function disease of anatomical entity 51
C0020179 Huntington Disease disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders Disease or Syndrome disease of anatomical entity 50
C0007117 Basal cell carcinoma disease Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation 49
C0019348 Herpes Simplex Infections group Infections; Skin and Connective Tissue Diseases Disease or Syndrome disease by infectious agent 49
C0036202 Sarcoidosis disease Hemic and Lymphatic Diseases Disease or Syndrome disease of anatomical entity 48
C0007138 Carcinoma, Transitional Cell disease Neoplasms Neoplastic Process disease of cellular proliferation 47
C0242383 Age related macular degeneration disease Eye Diseases Disease or Syndrome genetic disease; disease of anatomical entity 47
C1527336 Sjogren's Syndrome disease Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases Disease or Syndrome disease of anatomical entity 47
C0042373 Vascular Diseases group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 46
C0333641 Atrophic phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 46
C2937421 Prostatic Hyperplasia disease Male Urogenital Diseases Disease or Syndrome disease of anatomical entity; disease of cellular proliferation 46
C0025568 Metaplasia phenotype Pathological Conditions, Signs and Symptoms Cell or Molecular Dysfunction 45
C1176475 Ductal Carcinoma disease Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation 44
C0011884 Diabetic Retinopathy disease Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 43
C0334634 Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation 41
C3495559 Juvenile arthritis disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome disease of anatomical entity 40
C0007133 Carcinoma, Papillary disease Neoplasms Neoplastic Process disease of cellular proliferation 39
C0024301 Lymphoma, Follicular disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation 39
C0001815 Primary Myelofibrosis disease Hemic and Lymphatic Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation 38
C0015695 Fatty Liver disease Digestive System Diseases Disease or Syndrome genetic disease; disease of metabolism 37