Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C2930930 Abdominal obesity metabolic syndrome disease Nutritional and Metabolic Diseases Disease or Syndrome 1
C0000737 Abdominal Pain phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom Abnormality of the digestive system; Constitutional symptom 1
C0000880 Acanthamoeba Keratitis disease Infections; Eye Diseases Disease or Syndrome 1
C0001249 Actinobacillus Infections disease Infections Disease or Syndrome disease of anatomical entity; disease by infectious agent 1
C0149514 Acute bronchitis disease Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity Abnormality of the respiratory system 1
C0023479 Acute myelomonocytic leukemia disease Neoplasms Neoplastic Process Abnormality of the immune system; Neoplasm; Abnormality of blood and blood-forming tissues 1
C0023487 Acute Promyelocytic Leukemia disease Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation Abnormality of the immune system; Neoplasm; Abnormality of blood and blood-forming tissues 1
C1735373 Acute uveitis disease Disease or Syndrome 1
C0032580 Adenomatous Polyposis Coli disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms Neoplastic Process genetic disease 1
C0041755 Adverse reaction to drug group Chemically-Induced Disorders Pathologic Function 1
C0041228 African Trypanosomiasis disease Infections Disease or Syndrome disease by infectious agent 1
C0001849 AIDS Dementia Complex disease Infections; Immune System Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 1
C0078911 AIDS-Associated Nephropathy disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 1
C2717792 Airway Remodeling phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 1
C0001916 Albinism disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of the integument 1
C0078918 Albinism, Oculocutaneous disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases Congenital Abnormality genetic disease 1
C0270985 Alcohol myopathy disease Musculoskeletal Diseases; Nervous System Diseases; Chemically-Induced Disorders; Mental Disorders Disease or Syndrome 1
C0751865 Alcohol-Induced Disorders, Nervous System disease Nervous System Diseases; Chemically-Induced Disorders Disease or Syndrome 1
C0559469 Allergy to eggs phenotype Immune System Diseases Disease or Syndrome disease of anatomical entity 1
C0205710 Alpers Syndrome (disorder) disease Immune System Diseases; Nervous System Diseases Disease or Syndrome genetic disease; disease of metabolism; disease of anatomical entity 1
C0002351 Altitude Sickness phenotype Respiratory Tract Diseases Disease or Syndrome 1
C0002418 Amblyopia phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the eye 1
C0039585 Androgen-Insensitivity Syndrome disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome disease of anatomical entity 1
C0002895 Anemia, Sickle Cell disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome genetic disease; disease of anatomical entity 1
C0178417 Anhedonia disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction Abnormality of the nervous system 1