Pallor
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
124
|
4
|
0.100 |
None |
|
0 |
|
|
|
Hepatomegaly
|
phenotype |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Finding
|
523
|
30
|
0.100 |
None |
|
0 |
|
|
|
Abnormal bone structure
|
disease |
|
Anatomical Abnormality
|
7
|
|
0.100 |
None |
|
0 |
|
|
|
Splenomegaly
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
345
|
19
|
0.100 |
None |
|
0 |
|
|
|
Persistence of hemoglobin F
|
phenotype |
|
Finding
|
9
|
|
0.100 |
None |
|
0 |
|
|
|
Congenital Methemoglobinemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
6
|
8
|
0.010 |
None |
1.000 |
1 |
1
|
1972 |
1972 |
Erythrocytosis familial, 1
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
29
|
14
|
0.010 |
None |
1.000 |
1 |
|
1972 |
1972 |
Familial erythrocytosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
17
|
2
|
0.010 |
None |
1.000 |
1 |
|
1972 |
1972 |
Acute kidney injury
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Injury or Poisoning
|
185
|
3
|
0.300 |
None |
1.000 |
2 |
|
1977 |
1977 |
Kidney Failure, Acute
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
826
|
32
|
0.300 |
None |
1.000 |
2 |
|
1977 |
1977 |
Acute Kidney Insufficiency
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
104
|
|
0.300 |
None |
1.000 |
2 |
|
1977 |
1977 |
Oliguria
|
phenotype |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
24
|
|
0.300 |
None |
1.000 |
1 |
|
1977 |
1977 |
delta beta^0^ Thalassemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
10
|
|
0.010 |
None |
1.000 |
1 |
|
1979 |
1979 |
Deficiency of glucose-6-phosphate dehydrogenase
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
75
|
20
|
0.010 |
None |
1.000 |
1 |
|
1981 |
1981 |
Severe beta thalassemia
|
disease |
|
Disease or Syndrome
|
9
|
|
0.010 |
None |
1.000 |
1 |
|
1982 |
1982 |
Delta-Beta Thalassemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
12
|
|
0.030 |
None |
0.667 |
3 |
|
1982 |
1985 |
Gamma thalassemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
1987 |
1987 |
Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
32
|
5
|
0.010 |
None |
1.000 |
1 |
|
1988 |
1988 |
Dominant beta-thalassemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
5
|
2
|
0.010 |
None |
1.000 |
1 |
|
1988 |
1988 |
Polycythemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
82
|
22
|
0.010 |
None |
1.000 |
1 |
1
|
1989 |
1989 |
Idiopathic pulmonary hypertension
|
disease |
Respiratory Tract Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
161
|
5
|
0.010 |
None |
1.000 |
1 |
|
1991 |
1991 |
Sicca Syndrome
|
disease |
Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases
|
Disease or Syndrome
|
132
|
4
|
0.010 |
None |
1.000 |
1 |
|
1991 |
1991 |
Sweet Syndrome
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
104
|
3
|
0.010 |
None |
1.000 |
1 |
|
1991 |
1991 |
synovial sarcoma
|
disease |
Neoplasms
|
Neoplastic Process
|
299
|
4
|
0.010 |
None |
1.000 |
1 |
|
1991 |
1991 |
Homozygous alpha thalassemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
19
|
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |