Deficiency of pyruvate kinase
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
10
|
63
|
1.000 |
strong |
1.000 |
53 |
62
|
1991 |
2019 |
Adenosine Triphosphate, Elevated, Of Erythrocytes
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
1
|
3
|
0.600 |
None |
1.000 |
1 |
3
|
1997 |
1997 |
Diabetes Mellitus, Experimental
|
disease |
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Experimental Model of Disease
|
522
|
|
0.500 |
None |
1.000 |
2 |
|
2006 |
2010 |
Enzymopathy
|
group |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
17
|
1
|
0.300 |
strong |
1.000 |
2 |
|
1991 |
1996 |
Alloxan Diabetes
|
disease |
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Experimental Model of Disease
|
112
|
|
0.300 |
None |
1.000 |
1 |
|
2010 |
2010 |
Liver Cirrhosis, Experimental
|
disease |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Experimental Model of Disease
|
870
|
|
0.300 |
None |
1.000 |
1 |
|
2014 |
2014 |
Streptozotocin Diabetes
|
disease |
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Experimental Model of Disease
|
112
|
|
0.300 |
None |
1.000 |
1 |
|
2010 |
2010 |
Erythrocytosis familial, 1
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
29
|
14
|
0.300 |
None |
1.000 |
1 |
|
2012 |
2012 |
Malaria
|
disease |
Infections
|
Disease or Syndrome
|
685
|
148
|
0.240 |
None |
1.000 |
6 |
2
|
2003 |
2017 |
Reperfusion Injury
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Injury or Poisoning
|
300
|
|
0.200 |
None |
1.000 |
1 |
|
2006 |
2006 |
Hyperglycemia
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
1098
|
108
|
0.200 |
None |
1.000 |
1 |
|
1996 |
1996 |
Body Fat Distribution
|
phenotype |
|
Finding
|
90
|
119
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Reticulocyte count (procedure)
|
phenotype |
|
Laboratory Procedure
|
234
|
474
|
0.100 |
None |
1.000 |
1 |
2
|
2016 |
2016 |
Major Depressive Disorder
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
1236
|
1451
|
0.100 |
None |
1.000 |
1 |
1
|
2018 |
2018 |
Reticulocytosis
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
40
|
1
|
0.100 |
None |
|
0 |
|
|
|
Serum iron raised
|
phenotype |
Nutritional and Metabolic Diseases
|
Finding
|
10
|
|
0.100 |
None |
|
0 |
|
|
|
Anisocytosis
|
phenotype |
|
Finding
|
16
|
1
|
0.100 |
None |
|
0 |
|
|
|
Poikilocytosis
|
phenotype |
|
Finding
|
14
|
|
0.100 |
None |
|
0 |
|
|
|
Reduced red cell pyruvate kinase activity
|
phenotype |
|
Cell or Molecular Dysfunction
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Increased serum ferritin
|
phenotype |
|
Finding
|
23
|
1
|
0.100 |
None |
|
0 |
|
|
|
Chronic hemolytic anemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
15
|
5
|
0.100 |
None |
|
0 |
1
|
|
|
Neonatal unconjugated hyperbilirubinemia
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Disease or Syndrome
|
2
|
2
|
0.100 |
None |
|
0 |
1
|
|
|
Prolonged neonatal jaundice
|
phenotype |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Finding
|
59
|
14
|
0.100 |
None |
|
0 |
|
|
|
Anisocyte Measurement
|
phenotype |
|
Laboratory Procedure
|
15
|
|
0.100 |
None |
|
0 |
|
|
|
Reduced erythrocyte 2,3-diphosphoglycerate concentration
|
phenotype |
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
|
|
|