C1510586 |
Autism Spectrum Disorders
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
disease of mental health
|
Abnormality of the nervous system
|
53 |
C4277682 |
Chemical and Drug Induced Liver Injury
|
disease |
Digestive System Diseases; Chemically-Induced Disorders
|
Disease or Syndrome
|
|
|
53 |
C0009319 |
Colitis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the digestive system; Abnormality of the immune system
|
52 |
C0029866 |
Other ureteric obstruction
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Anatomical Abnormality
|
disease of anatomical entity
|
|
52 |
C0011854 |
Diabetes Mellitus, Insulin-Dependent
|
disease |
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
genetic disease; disease of metabolism
|
Abnormality of metabolism/homeostasis; Abnormality of the endocrine system
|
51 |
C0015695 |
Fatty Liver
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
genetic disease; disease of metabolism
|
|
51 |
C0151744 |
Myocardial Ischemia
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
50 |
C0023904 |
Liver Neoplasms, Experimental
|
phenotype |
Digestive System Diseases; Neoplasms
|
Neoplastic Process; Experimental Model of Disease
|
|
|
49 |
C0030567 |
Parkinson Disease
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
49 |
C0008370 |
Cholestasis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the digestive system
|
48 |
C0018129 |
Graft Rejection
|
phenotype |
|
Organ or Tissue Function
|
|
|
47 |
C0034069 |
Pulmonary Fibrosis
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the respiratory system
|
47 |
C0017658 |
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
|
46 |
C0011884 |
Diabetic Retinopathy
|
disease |
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
44 |
C0524620 |
Metabolic Syndrome X
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
genetic disease; syndrome
|
|
44 |
C0242706 |
Hyperoxia
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
|
|
42 |
C0024141 |
Lupus Erythematosus, Systemic
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the immune system
|
42 |
C0030193 |
Pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
|
Constitutional symptom
|
41 |
C0030305 |
Pancreatitis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the digestive system; Abnormality of the immune system
|
41 |
C0154860 |
Hereditary retinal dystrophy
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity; syndrome
|
|
40 |
C0024115 |
Lung diseases
|
group |
Respiratory Tract Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the respiratory system
|
40 |
C0038525 |
Subarachnoid Hemorrhage
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
|
Abnormality of the nervous system; Abnormality of blood and blood-forming tissues; Abnormality of the cardiovascular system
|
40 |
C0014544 |
Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the nervous system
|
39 |
C1332309 |
Anti-Basement Membrane Glomerulonephritis
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
38 |
C0022680 |
Polycystic Kidney Diseases
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity; syndrome
|
Abnormality of the genitourinary system
|
38 |