Source: ALL

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0264714 Acute heart failure disease Cardiovascular Diseases Disease or Syndrome 89 0
C0403416 Idiopathic crescentic glomerulonephritis disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system; Abnormality of the immune system 80 0
C0024713 Manic Disorder disease Mental Disorders Mental or Behavioral Dysfunction disease of mental health 76 0
C0267952 Fibrosis of pancreas disease Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 72 0
C0027720 Nephrosis disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity 68 0
C0241868 acute aortic dissection disease Cardiovascular Diseases Disease or Syndrome 63 0
C0549493 Alveolitis disease Skin and Connective Tissue Diseases; Respiratory Tract Diseases Disease or Syndrome 63 0
C0025261 Memory Disorders disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 62 0
C0017667 Nodular glomerulosclerosis disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 59 0
C4324563 Neutrophil extracellular trap formation disease Disease or Syndrome 55 0
C0221232 Welts phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases Sign or Symptom 53 0
C0029866 Other ureteric obstruction phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Anatomical Abnormality disease of anatomical entity 52 0
C0001622 Adrenal Gland Hyperfunction phenotype Endocrine System Diseases Disease or Syndrome disease of anatomical entity 50 0
C0242706 Hyperoxia phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0
C4021821 Abnormality of the urinary system disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome Abnormality of the genitourinary system 50 0
C4049993 Aristolochic Acid Nephropathy disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 49 0
C0917731 Male sterility phenotype Male Urogenital Diseases Finding 48 0
C0458219 Complex Regional Pain Syndromes disease Nervous System Diseases Disease or Syndrome disease of anatomical entity 47 0
C2960127 Heart failure with normal ejection fraction disease Cardiovascular Diseases Disease or Syndrome 47 0
C1609524 ADHF disease Disease or Syndrome 46 0
C0238421 Selenium deficiency disease Disease or Syndrome 44 0
C0272242 Complement deficiency disease group Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome disease of anatomical entity Abnormality of the immune system 42 0
C2882221 Acute pulmonary embolism disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 42 0
C0333997 Lymphoid hyperplasia disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 39 0
C0013182 Drug Allergy group Immune System Diseases; Chemically-Induced Disorders Pathologic Function 37 0