C0029866 |
Other ureteric obstruction
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Anatomical Abnormality
|
disease of anatomical entity
|
|
52 |
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 |
C0018129 |
Graft Rejection
|
phenotype |
|
Organ or Tissue Function
|
|
|
47 |
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 |
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 |
C0036982 |
Shock, Hemorrhagic
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
|
|
38 |
C1332309 |
Anti-Basement Membrane Glomerulonephritis
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
38 |
C0014556 |
Epilepsy, Temporal Lobe
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
36 |
C0160390 |
Injury of liver
|
disease |
Digestive System Diseases; Wounds and Injuries
|
Injury or Poisoning
|
|
|
36 |
C0555198 |
Malignant Glioma
|
disease |
Neoplasms
|
Neoplastic Process
|
disease of cellular proliferation
|
|
35 |
C0019284 |
Diaphragmatic Hernia
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
disease of anatomical entity
|
|
34 |
C0853897 |
Diabetic Cardiomyopathies
|
disease |
Endocrine System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
|
|
34 |
C2936380 |
Neointima
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
|
|
33 |
C0006142 |
Malignant neoplasm of breast
|
disease |
Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
|
32 |
C0027814 |
Neuritis, Autoimmune, Experimental
|
disease |
Immune System Diseases; Nervous System Diseases
|
Experimental Model of Disease
|
|
|
32 |
C0029531 |
Other cataract
|
disease |
Eye Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
32 |
C0267941 |
Pancreatitis, Acute Necrotizing
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
|
|
32 |
C0022116 |
Ischemia
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
disease of anatomical entity
|
|
30 |
C0027720 |
Nephrosis
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
29 |
C1415817 |
HETEROTAXY, VISCERAL, 2, AUTOSOMAL
|
disease |
|
Disease or Syndrome
|
physical disorder
|
|
29 |