Acid reflux
|
phenotype |
|
Finding
|
50
|
58
|
0.100 |
None |
|
0 |
1
|
|
|
Range of joint movement increased
|
phenotype |
|
Finding
|
30
|
46
|
0.100 |
None |
|
0 |
1
|
|
|
Central hypotonia
|
phenotype |
|
Finding
|
23
|
25
|
0.100 |
None |
|
0 |
1
|
|
|
Laryngeal cleft
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Anteverted nostril
|
phenotype |
|
Finding
|
30
|
35
|
0.100 |
None |
|
0 |
1
|
|
|
High, narrow palate
|
phenotype |
|
Finding
|
19
|
21
|
0.100 |
None |
|
0 |
1
|
|
|
Severe global developmental delay
|
phenotype |
|
Finding
|
33
|
50
|
0.100 |
None |
|
0 |
1
|
|
|
Poor suck
|
phenotype |
|
Finding
|
28
|
31
|
0.100 |
None |
|
0 |
1
|
|
|
Tracheomalacia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Respiratory Tract Diseases
|
Disease or Syndrome
|
5
|
5
|
0.100 |
None |
|
0 |
1
|
|
|
Hypoxemia
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
6
|
7
|
0.100 |
None |
|
0 |
1
|
|
|
Global developmental delay
|
disease |
|
Mental or Behavioral Dysfunction
|
303
|
505
|
0.100 |
None |
|
0 |
1
|
|
|
Sleep Apnea, Central
|
disease |
Respiratory Tract Diseases; Nervous System Diseases
|
Disease or Syndrome
|
6
|
7
|
0.100 |
None |
|
0 |
1
|
|
|
Sleep Apnea, Obstructive
|
disease |
Respiratory Tract Diseases; Nervous System Diseases
|
Disease or Syndrome
|
19
|
23
|
0.100 |
None |
|
0 |
1
|
|
|
Sagittal craniosynostosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
7
|
7
|
0.100 |
None |
|
0 |
1
|
|
|
Depressed nasal bridge
|
phenotype |
|
Finding
|
31
|
39
|
0.100 |
None |
|
0 |
1
|
|
|
Facial hypotonia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
6
|
6
|
0.100 |
None |
|
0 |
1
|
|
|
Periventricular gray matter heterotopia
|
disease |
|
Disease or Syndrome
|
2
|
3
|
0.100 |
None |
|
0 |
1
|
|
|
Neonatal respiratory distress
|
phenotype |
Respiratory Tract Diseases
|
Finding
|
31
|
34
|
0.100 |
None |
|
0 |
1
|
|
|
Cortical visual impairment
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Pathologic Function
|
21
|
27
|
0.100 |
None |
|
0 |
1
|
|
|
Localized hirsutism
|
phenotype |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Finding
|
2
|
2
|
0.100 |
None |
|
0 |
1
|
|
|
Nasogastric tube feeding in infancy
|
phenotype |
|
Finding
|
7
|
9
|
0.100 |
None |
|
0 |
1
|
|
|
Gastrostomy tube feeding in infancy
|
phenotype |
|
Finding
|
15
|
19
|
0.100 |
None |
|
0 |
1
|
|
|
Cerebral white matter hypoplasia
|
phenotype |
|
Finding
|
3
|
3
|
0.100 |
None |
|
0 |
1
|
|
|
Bilateral camptodactyly
|
disease |
|
Congenital Abnormality
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Contracture of the proximal interphalangeal joint of the 3rd finger
|
phenotype |
|
Anatomical Abnormality
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|