Aneurysm of aortic root
|
disease |
Cardiovascular Diseases
|
Anatomical Abnormality
|
39
|
15
|
0.100 |
None |
|
0 |
1
|
|
|
Dermal translucency
|
phenotype |
|
Finding
|
10
|
2
|
0.100 |
None |
|
0 |
|
|
|
Uterine Rupture
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications; Wounds and Injuries
|
Pathologic Function
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
Pneumothorax
|
phenotype |
Respiratory Tract Diseases
|
Disease or Syndrome
|
69
|
3
|
0.100 |
None |
|
0 |
|
|
|
Aneurysm of descending thoracic aorta
|
phenotype |
Cardiovascular Diseases
|
Anatomical Abnormality
|
15
|
|
0.100 |
None |
|
0 |
|
|
|
Tricuspid Valve Prolapse
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
13
|
4
|
0.100 |
None |
|
0 |
1
|
|
|
Tooth Crowding
|
phenotype |
Stomatognathic Diseases
|
Finding
|
82
|
19
|
0.100 |
None |
|
0 |
1
|
|
|
Acquired Camptodactyly
|
disease |
|
Acquired Abnormality
|
120
|
1
|
0.100 |
None |
|
0 |
|
|
|
Scoliosis, unspecified
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
850
|
135
|
0.100 |
None |
|
0 |
|
|
|
Skin Abnormalities
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
106
|
16
|
0.100 |
None |
|
0 |
|
|
|
Joint laxity
|
phenotype |
Musculoskeletal Diseases
|
Pathologic Function
|
224
|
15
|
0.100 |
None |
|
0 |
|
|
|
Generalized arterial tortuosity
|
phenotype |
|
Finding
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
Range of joint movement increased
|
phenotype |
|
Finding
|
30
|
46
|
0.100 |
None |
|
0 |
1
|
|
|
Osteoarthrosis, localized, not specified whether primary or secondary
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
28
|
|
0.200 |
None |
|
0 |
|
|
|
Pulmonary artery aneurysm
|
phenotype |
Cardiovascular Diseases
|
Pathologic Function
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
Ischemic stroke
|
disease |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1159
|
704
|
0.100 |
None |
|
0 |
|
|
|
Linear atrophy
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
149
|
6
|
0.100 |
None |
|
0 |
|
|
|
Soft skin
|
phenotype |
|
Finding
|
22
|
3
|
0.100 |
None |
|
0 |
|
|
|
Micrognathism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
|
Congenital Abnormality
|
586
|
53
|
0.100 |
None |
|
0 |
|
|
|
Disproportionate tall stature
|
phenotype |
|
Finding
|
30
|
17
|
0.100 |
None |
|
0 |
1
|
|
|
Ascending aortic dissection
|
phenotype |
Cardiovascular Diseases
|
Disease or Syndrome
|
25
|
1
|
0.100 |
None |
|
0 |
|
|
|
Myopia
|
disease |
Eye Diseases
|
Disease or Syndrome
|
490
|
167
|
0.100 |
None |
|
0 |
1
|
|
|
Subarachnoid Hemorrhage
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
501
|
26
|
0.100 |
None |
|
0 |
|
|
|
Chest Pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
154
|
7
|
0.100 |
None |
|
0 |
|
|
|
Flexion contracture of proximal interphalangeal joint
|
phenotype |
|
Finding
|
168
|
7
|
0.100 |
None |
|
0 |
|
|
|