Source: CTD_mouse

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0271650 Impaired glucose tolerance phenotype Nutritional and Metabolic Diseases Disease or Syndrome disease of metabolism 2
C0021655 Insulin Resistance phenotype Nutritional and Metabolic Diseases Pathologic Function Abnormality of metabolism/homeostasis 2
C0920563 Insulin Sensitivity phenotype Nutritional and Metabolic Diseases Pathologic Function 2
C0022658 Kidney Diseases group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system 2
C0023903 Liver neoplasms group Digestive System Diseases; Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation Abnormality of the digestive system; Neoplasm 2
C0024115 Lung diseases group Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity Abnormality of the respiratory system 2
C0024121 Lung Neoplasms group Neoplasms; Respiratory Tract Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation Neoplasm; Abnormality of the respiratory system 2
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 2
C0242379 Malignant neoplasm of lung disease Neoplasms; Respiratory Tract Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation Neoplasm; Abnormality of the respiratory system 2
C1257925 Mammary Carcinoma, Animal disease Neoplasms; Animal Diseases Neoplastic Process 2
C0036529 Myocardial Diseases, Secondary group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 2
C0027540 Necrosis phenotype Pathological Conditions, Signs and Symptoms Organ or Tissue Function 2
C0027659 Neoplasms, Experimental phenotype Neoplasms Neoplastic Process; Experimental Model of Disease 2
C0027746 Nerve Degeneration phenotype Pathological Conditions, Signs and Symptoms Cell or Molecular Dysfunction Abnormality of the nervous system 2
C0035126 Reperfusion Injury disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Injury or Poisoning 2
C0205698 Undifferentiated carcinoma disease Neoplasms Neoplastic Process 2
C4316903 Absence Seizures phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome Abnormality of the nervous system 1
C0234238 Ache phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 1
C2609414 Acute kidney injury disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Injury or Poisoning disease of anatomical entity Abnormality of the genitourinary system 1
C1565662 Acute Kidney Insufficiency disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity 1
C1879321 Acute Myeloid Leukemia (AML-M2) disease Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation 1
C0026998 Acute Myeloid Leukemia, M1 disease Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation 1
C0001418 Adenocarcinoma group Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation 1
C0205641 Adenocarcinoma, Basal Cell disease Neoplasms Neoplastic Process 1
C0205642 Adenocarcinoma, Oxyphilic disease Neoplasms Neoplastic Process 1