ELLIPTOCYTOSIS 3
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
1
|
9
|
0.600 |
strong |
1.000 |
4 |
9
|
1990 |
1995 |
ANEMIA, PERINATAL HEMOLYTIC, FATAL OR NEAR-FATAL
|
disease |
|
Finding
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Anemia, hereditary spherocytic hemolytic
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
5
|
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
Leptin measurement
|
phenotype |
|
Laboratory Procedure
|
5
|
9
|
0.100 |
None |
1.000 |
1 |
1
|
2012 |
2012 |
Spherocytosis
|
phenotype |
|
Finding
|
5
|
|
0.100 |
None |
|
0 |
|
|
|
Anemia, Neonatal
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
6
|
|
0.300 |
None |
1.000 |
1 |
|
1997 |
1997 |
Spontaneous hemolytic crises
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
7
|
|
0.100 |
None |
|
0 |
|
|
|
SPHEROCYTOSIS, HEREDITARY, 2
|
disease |
|
Disease or Syndrome
|
8
|
13
|
0.700 |
strong |
1.000 |
8 |
13
|
1993 |
2016 |
Increased red cell osmotic fragility
|
phenotype |
|
Finding
|
9
|
|
0.100 |
None |
|
0 |
|
|
|
Elliptocytosis found
|
phenotype |
|
Finding
|
12
|
|
0.400 |
strong |
1.000 |
2 |
|
1993 |
2016 |
Anemia, Microangiopathic
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
13
|
|
0.300 |
None |
1.000 |
1 |
|
1997 |
1997 |
Stomatocytosis Result
|
phenotype |
|
Laboratory or Test Result
|
13
|
|
0.100 |
None |
|
0 |
|
|
|
Increased mean corpuscular hemoglobin concentration
|
phenotype |
|
Finding
|
13
|
|
0.100 |
None |
|
0 |
|
|
|
stomatocytic anemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
15
|
1
|
0.100 |
None |
|
0 |
|
|
|
Anemia, Hemolytic, Acquired
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
16
|
1
|
0.300 |
None |
1.000 |
1 |
|
1997 |
1997 |
Extramedullary Hematopoiesis Function
|
phenotype |
|
Organ or Tissue Function
|
16
|
|
0.100 |
None |
|
0 |
|
|
|
Maculopapular Lesion
|
phenotype |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases
|
Finding
|
16
|
28
|
0.100 |
None |
|
0 |
|
|
|
Elliptocytosis, Hereditary
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
23
|
1
|
0.750 |
strong |
1.000 |
9 |
|
1990 |
2016 |
Anemia, Hemolytic, Congenital
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
27
|
8
|
0.100 |
None |
|
0 |
|
|
|
Microangiopathic hemolytic anemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
31
|
|
0.300 |
None |
1.000 |
1 |
|
1997 |
1997 |
Hyperbilirubinemia, Neonatal
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Disease or Syndrome
|
33
|
15
|
0.100 |
None |
|
0 |
|
|
|
Chills
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
34
|
|
0.100 |
None |
|
0 |
|
|
|
Focal nodular hyperplasia of liver
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
39
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Reticulocytosis
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
40
|
1
|
0.100 |
None |
|
0 |
|
|
|
Restrictive cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
41
|
30
|
0.100 |
None |
|
0 |
|
|
|