Source: CURATED

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C1257931 Mammary Neoplasms, Human disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 525 0
C4704874 Mammary Carcinoma, Human disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 525 0
C0019193 Hepatitis, Toxic disease Digestive System Diseases; Chemically-Induced Disorders Injury or Poisoning 404 0
C1262760 Hepatitis, Drug-Induced disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404 0
C3658290 Drug-Induced Acute Liver Injury disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404 0
C4279912 Chemically-Induced Liver Toxicity disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 404 0
C0027627 Neoplasm Metastasis phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 217 0
C0027626 Neoplasm Invasiveness phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Pathologic Function 184 0
C0023903 Liver neoplasms group Digestive System Diseases; Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation Abnormality of the digestive system; Neoplasm 142 0
C0345904 Malignant neoplasm of liver disease Digestive System Diseases; Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation Abnormality of the digestive system; Neoplasm 142 0
C0021368 Inflammation phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 127 0
C0000786 Spontaneous abortion phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function Abnormality of prenatal development or birth 109 0
C0000822 Abortion, Tubal phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 109 0
C3830362 Early Pregnancy Loss phenotype Female Urogenital Diseases and Pregnancy Complications Finding 109 0
C4552766 Miscarriage disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 109 0
C0023895 Liver diseases group Digestive System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the digestive system 72 0
C0086565 Liver Dysfunction phenotype Digestive System Diseases Finding Abnormality of the digestive system 72 0
C0011616 Contact Dermatitis disease Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity 71 0
C0162351 Contact hypersensitivity phenotype Skin and Connective Tissue Diseases Pathologic Function 71 0
C0086692 Benign Neoplasm group Neoplasms Neoplastic Process 68 0
C0027659 Neoplasms, Experimental phenotype Neoplasms Neoplastic Process; Experimental Model of Disease 66 0
C0920563 Insulin Sensitivity phenotype Nutritional and Metabolic Diseases Pathologic Function 60 0
C1563937 Atherogenesis phenotype Cardiovascular Diseases Pathologic Function 59 0
C0027540 Necrosis phenotype Pathological Conditions, Signs and Symptoms Organ or Tissue Function 55 0
C0032300 Lobar Pneumonia disease Infections; Respiratory Tract Diseases Disease or Syndrome 54 0