Nasal bridge wide
|
phenotype |
|
Finding
|
429
|
29
|
0.100 |
None |
|
0 |
|
|
|
Aplasia/Hypoplasia of the earlobes
|
disease |
|
Congenital Abnormality
|
11
|
|
0.100 |
None |
|
0 |
|
|
|
Low-set, posteriorly rotated ears
|
phenotype |
|
Finding
|
223
|
19
|
0.100 |
None |
|
0 |
|
|
|
Malar flattening
|
disease |
|
Anatomical Abnormality
|
190
|
12
|
0.100 |
None |
|
0 |
|
|
|
Underdeveloped supraorbital ridges
|
phenotype |
|
Finding
|
53
|
2
|
0.100 |
None |
|
0 |
|
|
|
Heinz-Ehrlich Body Measurement
|
phenotype |
|
Laboratory Procedure
|
6
|
|
0.100 |
None |
|
0 |
|
|
|
Short Stature, CTCAE
|
phenotype |
|
Finding
|
1010
|
|
0.100 |
None |
|
0 |
|
|
|
HEMOGLOBIN H DISEASE, NONDELETIONAL
|
disease |
|
Disease or Syndrome
|
2
|
10
|
0.100 |
None |
|
0 |
2
|
|
|
Abnormality of metabolism/homeostasis
|
phenotype |
|
Finding
|
171
|
5
|
0.100 |
None |
|
0 |
|
|
|
Aplasia/Hypoplasia of the eyebrow
|
phenotype |
|
Finding
|
52
|
|
0.100 |
None |
|
0 |
|
|
|
Reduced alpha/beta synthesis ratio
|
phenotype |
|
Finding
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
HEMOGLOBIN EVANSTON PHENOTYPE
|
phenotype |
|
Finding
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
ERYTHROCYTOSIS, FAMILIAL, 7
|
disease |
|
Disease or Syndrome
|
2
|
12
|
0.100 |
None |
|
0 |
8
|
|
|
Cardiac Arrest
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
411
|
50
|
0.050 |
None |
1.000 |
5 |
|
1993 |
2019 |
Cardiovascular Diseases
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
1756
|
711
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Hypertensive disease
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
2322
|
1085
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Vascular Diseases
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
688
|
40
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Myocardial Ischemia
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
756
|
103
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Congestive heart failure
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1760
|
165
|
0.100 |
None |
|
0 |
|
|
|
Pericarditis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
51
|
6
|
0.100 |
None |
|
0 |
|
|
|
Familial Mediterranean Fever
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Disease or Syndrome
|
133
|
82
|
0.020 |
None |
1.000 |
2 |
|
1992 |
1993 |
Congenital Abnormality
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
1098
|
73
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Cystic Fibrosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases
|
Disease or Syndrome
|
852
|
704
|
0.020 |
None |
1.000 |
2 |
|
1983 |
2003 |
Hemolytic disorder
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
15
|
|
0.010 |
None |
1.000 |
1 |
|
1994 |
1994 |
Polycystic Kidney, Autosomal Dominant
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
280
|
35
|
0.100 |
None |
1.000 |
11 |
|
1985 |
1992 |