Source: LHGDN

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0032371 Poliomyelitis disease Infections; Nervous System Diseases Disease or Syndrome disease of anatomical entity; disease by infectious agent 1
C0948031 Primary Graft Dysfunction phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 2
C0026780 Mumps disease Infections; Stomatognathic Diseases Disease or Syndrome disease of anatomical entity; disease by infectious agent 3
C0025289 Meningitis disease Nervous System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the nervous system; Abnormality of the immune system 4
C0032533 Polymyalgia Rheumatica disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome disease of anatomical entity 4
C0040147 Thyroiditis disease Endocrine System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the endocrine system; Abnormality of the immune system 5
C0008313 Cholangitis, Sclerosing disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system; Abnormality of the immune system 7
C0162429 Malnutrition disease Nutritional and Metabolic Diseases Disease or Syndrome disease of metabolism Abnormality of the digestive system 7
C0040021 Thromboangiitis Obliterans disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 7
C0025297 Viral meningitis disease Infections; Nervous System Diseases Disease or Syndrome disease of anatomical entity 7
C0009088 Cluster Headache disease Nervous System Diseases Disease or Syndrome Abnormality of the nervous system 8
C0029458 Osteoporosis, Postmenopausal disease Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome disease of anatomical entity 9
C0036330 Schistosomiasis mansoni disease Infections Disease or Syndrome disease by infectious agent 9
C0019100 Severe Dengue disease Infections Disease or Syndrome disease by infectious agent 9
C0005411 Biliary Atresia disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality disease of anatomical entity Abnormality of the digestive system 10
C0035436 Rheumatic Fever disease Infections; Musculoskeletal Diseases Disease or Syndrome disease by infectious agent 10
C0002986 Fabry Disease disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome genetic disease; disease of metabolism Abnormality of the integument; Abnormality of the cardiovascular system 11
C0033847 Pseudoxanthoma Elasticum disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome genetic disease; disease of anatomical entity 11
C0002171 Alopecia Areata disease Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity Abnormality of the integument 12
C0030805 Bullous pemphigoid disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome disease of anatomical entity 12
C0006271 Bronchiolitis disease Infections; Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity Abnormality of the immune system; Abnormality of the respiratory system 14
C0242231 Coronary Stenosis disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 14
C0393571 Multiple System Atrophy phenotype Nervous System Diseases Pathologic Function disease of anatomical entity 15
C0022876 Premature Obstetric Labor phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 16
C0852036 Pregnancy associated hypertension phenotype Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 17