Source: ALL

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0235710 Chest discomfort phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 2 0
C0263779 Interphalangeal osteoarthritis disease Musculoskeletal Diseases Disease or Syndrome 2 0
C0264949 Burn shock phenotype Pathological Conditions, Signs and Symptoms; Wounds and Injuries Disease or Syndrome 2 0
C0340169 Simple pneumoconiosis disease Respiratory Tract Diseases; Occupational Diseases Disease or Syndrome 2 0
C0346342 Carcinoma ex pleomorphic adenoma of lacrimal gland disease Neoplastic Process disease of anatomical entity; disease of cellular proliferation 2 0
C0751008 Intracranial Arteriovenous Malformation, Ruptured disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases Congenital Abnormality 2 0
C0848538 fluid retention in lung phenotype Sign or Symptom 2 0
C1168186 Septicopyemia disease Disease or Syndrome 2 0
C1262202 Lymphocytic alveolitis disease Disease or Syndrome 2 0
C1274377 Vibrio vulnificus infection disease Infections Disease or Syndrome 2 0
C1332293 Castleman Disease, Hyaline-Vascular Type disease Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 2 0
C1562893 Retrocorneal fibrous membrane disease Eye Diseases Disease or Syndrome 2 0
C1706527 Primary intraocular non-Hodgkin malignant lymphoma disease Neoplastic Process 2 0
C3640014 Unbearable Pain phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 2 0
C3888846 Hyperosmolar Hyperglycemic State disease Endocrine System Diseases Disease or Syndrome 2 0
C0242699 Bone Demineralization, Pathologic disease Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 3 3
C0406735 Hypoplastic enamel-onycholysis-hypohidrosis syndrome disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Disease or Syndrome syndrome 3 2
C0151828 Injection site pain phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Chemically-Induced Disorders Sign or Symptom 3 0
C0206615 Pneumovirus Infections group Infections Disease or Syndrome 3 0
C0221276 Relative erythrocytosis disease Hemic and Lymphatic Diseases Disease or Syndrome genetic disease; disease of anatomical entity 3 0
C0268405 Hemodialysis-associated amyloidosis disease Nutritional and Metabolic Diseases Disease or Syndrome 3 0
C0270718 Arrested hydrocephalus disease Nervous System Diseases Disease or Syndrome 3 0
C0276108 Chlamydia psittaci infection disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome disease by infectious agent 3 0
C0281774 Acute psychosis disease Mental Disorders Mental or Behavioral Dysfunction 3 0
C0282507 Heat Stress Disorders phenotype Wounds and Injuries Injury or Poisoning 3 0