Source: ALL

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C2919142 Short Stature, CTCAE phenotype Finding 1010 0
C0023893 Liver Cirrhosis, Experimental disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Experimental Model of Disease 870 0
C1963184 Nystagmus, CTCAE 3.0 phenotype Finding 779 0
C4554036 Nystagmus, CTCAE 5.0 phenotype Finding 779 0
C0740391 Middle Cerebral Artery Occlusion disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 626 0
C4704874 Mammary Carcinoma, Human disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 545 0
C1257931 Mammary Neoplasms, Human disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 527 0
C0011853 Diabetes Mellitus, Experimental disease Nutritional and Metabolic Diseases; Endocrine System Diseases Experimental Model of Disease 522 0
C3714514 Infection group Infections Pathologic Function 491 0
C4553743 Spasticity, CTCAE phenotype Finding 477 0
C0021368 Inflammation phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 467 0
C3665347 Visual Impairment phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Finding Abnormality of the eye 422 0
C1262760 Hepatitis, Drug-Induced disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 418 0
C3658290 Drug-Induced Acute Liver Injury disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 413 0
C0019193 Hepatitis, Toxic disease Digestive System Diseases; Chemically-Induced Disorders Injury or Poisoning 412 0
C4279912 Chemically-Induced Liver Toxicity disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 412 0
C1531647 Cerebral ventriculomegaly phenotype Nervous System Diseases Finding disease of anatomical entity 410 0
C0041956 Ureteral obstruction phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system 359 0
C1318485 Liver regeneration disorder phenotype Digestive System Diseases Disease or Syndrome Abnormality of the digestive system 346 0
C1969372 Tubulointerstitial fibrosis phenotype Disease or Syndrome Abnormality of the genitourinary system 328 0
C1861403 Variable expressivity phenotype Finding 319 0
C0151888 Hyporeflexia phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 312 0
C0035126 Reperfusion Injury disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Injury or Poisoning 300 0
C4551915 Gait Disturbance, CTCAE phenotype Finding 299 0
C0003130 Anoxia phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 287 0