Source: ALL

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0000727 Abdomen, Acute phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 2 0
C0000729 Abdominal Cramps phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities Sign or Symptom 1 0
C0000731 Abdomen distended phenotype Digestive System Diseases Finding Abnormality of the digestive system 103 6
C0000734 Abdominal mass phenotype Digestive System Diseases Finding Abnormality of the digestive system 2 0
C0000735 Abdominal Neoplasms group Neoplasms Neoplastic Process 13 0
C0000737 Abdominal Pain phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom Abnormality of the digestive system; Constitutional symptom 302 18
C0000744 Abetalipoproteinemia disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome genetic disease; disease of metabolism Abnormality of metabolism/homeostasis 65 19
C0000768 Congenital Abnormality group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 1098 73
C0000771 Abnormalities, Drug-Induced group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 5 0
C0000772 Multiple congenital anomalies group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 251 350
C0000786 Spontaneous abortion phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function Abnormality of prenatal development or birth 188 0
C0000809 Abortion, Habitual disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 7 0
C0000821 Threatened abortion phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function disease of anatomical entity 1 0
C0000822 Abortion, Tubal phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 109 0
C0000832 Abruptio Placentae phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function disease of anatomical entity Abnormality of prenatal development or birth 12 0
C0000833 Abscess phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 96 1
C0000846 Agenesis disease Congenital Abnormality 161 44
C0000880 Acanthamoeba Keratitis disease Infections; Eye Diseases Disease or Syndrome 22 0
C0000887 Acantholysis phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Pathologic Function Abnormality of the integument 11 0
C0000889 Acanthosis Nigricans disease Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity Abnormality of the integument 64 11
C0000921 Accidental Falls phenotype Injury or Poisoning 22 0
C0001075 Achlorhydria phenotype Digestive System Diseases; Nutritional and Metabolic Diseases Pathologic Function 5 0
C0001079 Achondrogenesis disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 4 0
C0001080 Achondroplasia disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality genetic disease; disease of anatomical entity 46 21
C0001122 Acidosis phenotype Nutritional and Metabolic Diseases Pathologic Function disease of metabolism Abnormality of metabolism/homeostasis 28 0