Familial hemorrhagic diathesis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
1982 |
1982 |
Alpha-2-antiplasmin deficiency
|
disease |
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
1982 |
1982 |
Olfaction Disorders
|
group |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
2
|
|
0.200 |
None |
1.000 |
1 |
|
2013 |
2013 |
Osteogenesis Imperfecta, Type VI
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
3
|
6
|
0.900 |
strong |
1.000 |
16 |
6
|
2011 |
2019 |
Myopia, Progressive
|
disease |
Eye Diseases
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Fibrin thrombus
|
disease |
Cardiovascular Diseases
|
Acquired Abnormality
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Osteogenesis imperfecta, type 5
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
4
|
3
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Pancreatic steatosis
|
disease |
|
Disease or Syndrome
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Diabetic keratopathy
|
disease |
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Corneal Sensitivity
|
phenotype |
|
Sign or Symptom
|
8
|
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2018 |
Visually threatening diabetic retinopathy
|
disease |
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
8
|
4
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Hypoplasminogenemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
9
|
3
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Protrusio acetabuli
|
disease |
|
Anatomical Abnormality
|
10
|
2
|
0.100 |
None |
|
0 |
|
|
|
Osteogenesis imperfecta type IV (disorder)
|
disease |
|
Disease or Syndrome; Congenital Abnormality
|
12
|
65
|
0.300 |
None |
1.000 |
1 |
|
2015 |
2015 |
Thromboembolic stroke
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
13
|
1
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Beaking of vertebral bodies
|
phenotype |
|
Finding
|
13
|
|
0.100 |
None |
|
0 |
|
|
|
Biconcave vertebral bodies
|
phenotype |
|
Finding
|
16
|
|
0.100 |
None |
|
0 |
|
|
|
Osteogenesis imperfecta type III (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
18
|
67
|
0.300 |
None |
1.000 |
2 |
|
2011 |
2015 |
Avascular retina
|
disease |
|
Disease or Syndrome
|
19
|
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
20
|
2
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |
Wet age-related macular degeneration
|
disease |
|
Disease or Syndrome
|
20
|
2
|
0.010 |
None |
1.000 |
1 |
1
|
2008 |
2008 |
Glaucoma, Neovascular
|
disease |
Eye Diseases
|
Disease or Syndrome
|
23
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Meibomian gland dysfunction
|
disease |
Eye Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
23
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Eye Neoplasms
|
group |
Neoplasms; Eye Diseases
|
Neoplastic Process
|
24
|
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Leukostasis
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
25
|
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |