Scoliosis, unspecified
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
63
|
92
|
0.110 |
None |
1.000 |
0 |
1
|
2011 |
2011 |
Ventricular Septal Defects
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
31
|
34
|
0.110 |
None |
1.000 |
0 |
1
|
2007 |
2007 |
NOONAN SYNDROME 3
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
6
|
32
|
0.100 |
None |
1.000 |
81 |
16
|
2002 |
2016 |
Dysmorphic features
|
disease |
|
Congenital Abnormality
|
335
|
611
|
0.100 |
None |
1.000 |
20 |
7
|
1968 |
2016 |
Multiple congenital anomalies
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
237
|
350
|
0.100 |
None |
1.000 |
20 |
4
|
1968 |
2016 |
Congenital stenosis of pulmonary valve
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases
|
Congenital Abnormality
|
1
|
3
|
0.100 |
None |
1.000 |
10 |
3
|
2001 |
2012 |
Hypertrophic cardiomyopathy without obstruction
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
1
|
0.100 |
None |
1.000 |
7 |
1
|
2001 |
2007 |
Short stature
|
phenotype |
|
Finding
|
190
|
292
|
0.100 |
None |
1.000 |
7 |
14
|
2001 |
2008 |
Pediatric failure to thrive
|
disease |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Mental Disorders
|
Disease or Syndrome
|
89
|
118
|
0.100 |
None |
1.000 |
6 |
4
|
2001 |
2018 |
Low set ears
|
disease |
|
Congenital Abnormality
|
56
|
64
|
0.100 |
None |
1.000 |
6 |
5
|
2001 |
2009 |
Gastroesophageal reflux disease
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
2
|
2
|
0.100 |
None |
1.000 |
4 |
1
|
2003 |
2006 |
Septal hypertrophy
|
disease |
|
Acquired Abnormality
|
1
|
1
|
0.100 |
None |
1.000 |
4 |
1
|
2002 |
2009 |
Large head (disorder)
|
phenotype |
|
Finding
|
64
|
116
|
0.100 |
None |
1.000 |
4 |
1
|
2004 |
2006 |
Downward slant of palpebral fissure
|
phenotype |
|
Finding
|
35
|
49
|
0.100 |
None |
1.000 |
4 |
5
|
2002 |
2009 |
Narrow forehead
|
phenotype |
|
Finding
|
19
|
20
|
0.100 |
None |
1.000 |
4 |
1
|
2001 |
2012 |
Orbital separation excessive
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Finding
|
63
|
77
|
0.100 |
None |
1.000 |
4 |
13
|
2001 |
2006 |
Increased tendency to bruise
|
phenotype |
Wounds and Injuries
|
Finding
|
9
|
14
|
0.100 |
None |
1.000 |
4 |
4
|
2002 |
2009 |
Congenital insufficiency of pulmonary valve
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
1
|
1
|
0.100 |
None |
1.000 |
4 |
1
|
2001 |
2012 |
Dysplastic pulmonary valve
|
phenotype |
|
Finding
|
2
|
3
|
0.100 |
None |
1.000 |
3 |
2
|
2005 |
2018 |
Refractive amblyopia
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
1
|
1
|
0.100 |
None |
1.000 |
3 |
1
|
2002 |
2008 |
Astigmatism
|
disease |
Eye Diseases
|
Disease or Syndrome
|
15
|
14
|
0.100 |
None |
1.000 |
3 |
1
|
2002 |
2008 |
Curly hair (finding)
|
phenotype |
|
Finding
|
4
|
7
|
0.100 |
None |
1.000 |
2 |
1
|
2001 |
2005 |
Hypertensive disease
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
25
|
33
|
0.100 |
None |
1.000 |
2 |
1
|
2001 |
2006 |
Congenital ocular coloboma (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
11
|
11
|
0.100 |
None |
1.000 |
2 |
1
|
2001 |
2005 |
Multiple nevi
|
disease |
Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
1
|
1
|
0.100 |
None |
1.000 |
2 |
1
|
2001 |
2005 |