FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 6
|
phenotype |
|
Finding
|
1
|
3
|
0.400 |
moderate |
|
0 |
3
|
|
|
In(Lu) phenotype (finding)
|
phenotype |
|
Finding
|
1
|
10
|
0.400 |
moderate |
|
0 |
10
|
|
|
Congenital dyserythropoietic anemia, type II
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
21
|
14
|
0.300 |
None |
|
0 |
|
|
|
Congenital dyserythropoietic anemia, type I
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
8
|
12
|
0.300 |
None |
|
0 |
|
|
|
Congenital dyserythropoietic anemia, type III
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
6
|
|
0.300 |
None |
|
0 |
|
|
|
Abnormal bone structure
|
disease |
|
Anatomical Abnormality
|
7
|
|
0.100 |
None |
|
0 |
|
|
|
Short Stature, CTCAE
|
phenotype |
|
Finding
|
1010
|
|
0.100 |
None |
|
0 |
|
|
|
Persistence of hemoglobin F
|
phenotype |
|
Finding
|
9
|
|
0.100 |
None |
|
0 |
|
|
|
Hepatomegaly
|
phenotype |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Finding
|
523
|
30
|
0.100 |
None |
|
0 |
|
|
|
Pallor
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
124
|
4
|
0.100 |
None |
|
0 |
|
|
|
Hyperbilirubinemia
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
131
|
27
|
0.100 |
None |
|
0 |
|
|
|
Erythroid hyperplasia
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
22
|
3
|
0.100 |
None |
|
0 |
|
|
|
Dwarfism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
1261
|
77
|
0.100 |
None |
|
0 |
|
|
|
Blood group antigen abnormality
|
phenotype |
|
Anatomical Abnormality
|
8
|
6
|
0.100 |
None |
|
0 |
1
|
|
|
Absence of Lutheran antigen on erythrocytes
|
disease |
|
Anatomical Abnormality
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Anemia of inadequate production
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
10
|
3
|
0.100 |
None |
|
0 |
|
|
|
Reticulocytosis
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
40
|
1
|
0.100 |
None |
|
0 |
|
|
|
Short stature
|
phenotype |
|
Finding
|
1127
|
292
|
0.100 |
None |
|
0 |
|
|
|
Splenomegaly
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
345
|
19
|
0.100 |
None |
|
0 |
|
|
|
Hereditary spherocytosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
53
|
13
|
0.210 |
None |
1.000 |
1 |
|
2010 |
2010 |
Juvenile Myelomonocytic Leukemia
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
179
|
70
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Erythroblastosis
|
disease |
|
Disease or Syndrome
|
89
|
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
5q-syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
45
|
1
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Hemoglobin H Disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
29
|
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
IMMUNE SUPPRESSION
|
phenotype |
|
Disease or Syndrome
|
222
|
3
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |