CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0029291 Psittacosis disease Infections Disease or Syndrome disease by infectious agent 1 0
C0151536 Stenosis of bronchus disease Respiratory Tract Diseases Anatomical Abnormality 1 0
C0233599 Bar-biting disease Mental or Behavioral Dysfunction 1 0
C0235453 Steroid withdrawal syndrome disease Endocrine System Diseases Disease or Syndrome 1 0
C0235876 Depression aggravated phenotype Mental Disorders; Behavior and Behavior Mechanisms Sign or Symptom 1 0
C0238120 Acquired Factor XIII Deficiency disease Disease or Syndrome 1 0
C0238741 Upper back pain phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 1 0
C0272209 T lymphocyte disorder disease Disease or Syndrome 1 0
C0392441 Coup de sabre scleroderma disease Skin and Connective Tissue Diseases Disease or Syndrome 1 0
C0400943 Cirrhosis - non-alcoholic disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 1 0
C0438716 Chest pressure phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 1 0
C0751280 Cystic Periventricular Leukomalacia disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1 0
C0948279 Beta haemolytic streptococcal infection disease Infections Disease or Syndrome 1 0
C1858067 ASTHMA AND NASAL POLYPS disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 1 0
C1859694 Periarticular osteoporosis disease Disease or Syndrome 1 0
C3898582 Localized Castleman Disease disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 1 0
C4040834 Inflammation of fetal umbilical artery disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases Disease or Syndrome 1 0
C4505226 Gender-Based Violence disease Mental or Behavioral Dysfunction 1 0
C1969086 Tyrosine Kinase 2 Deficiency disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 2 7
C0264222 Acute upper respiratory infection disease Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases Disease or Syndrome 2 2
C0022906 Lacrimal Duct Obstruction disease Eye Diseases Anatomical Abnormality disease of anatomical entity Abnormality of head or neck 2 0
C0079238 Digestive System Fistula phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 2 0
C0086238 Secondary generalized epilepsy disease Nervous System Diseases Disease or Syndrome 2 0
C0149650 Chronic mastitis disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases Disease or Syndrome 2 0
C0152413 Pneumonia due to respiratory syncytial virus disease Infections; Respiratory Tract Diseases Disease or Syndrome 2 0