Keratoconus
|
disease |
Eye Diseases
|
Disease or Syndrome
|
269
|
83
|
0.500 |
None |
0.871 |
31 |
12
|
2002 |
2019 |
Keratoconus 1
|
disease |
Eye Diseases
|
Disease or Syndrome
|
2
|
28
|
0.700 |
None |
1.000 |
7 |
8
|
2002 |
2011 |
Polymorphous corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
14
|
4
|
0.400 |
None |
1.000 |
18 |
3
|
2002 |
2019 |
Age related macular degeneration
|
disease |
Eye Diseases
|
Disease or Syndrome
|
685
|
663
|
0.010 |
None |
1.000 |
1 |
1
|
2006 |
2006 |
Macular degeneration
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
44
|
16
|
0.010 |
None |
1.000 |
1 |
1
|
2006 |
2006 |
CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME
|
disease |
|
Disease or Syndrome
|
1
|
1
|
0.700 |
moderate |
1.000 |
1 |
1
|
2004 |
2004 |
Tuberculosis
|
disease |
Infections
|
Disease or Syndrome
|
1256
|
328
|
0.100 |
None |
0.941 |
17 |
|
1996 |
2019 |
CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
12
|
4
|
0.360 |
moderate |
0.857 |
7 |
|
2004 |
2018 |
Corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
113
|
25
|
0.030 |
None |
1.000 |
3 |
|
2002 |
2010 |
Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
10161
|
1644
|
0.030 |
None |
1.000 |
3 |
|
2008 |
2019 |
Progressive pseudorheumatoid dysplasia
|
disease |
Musculoskeletal Diseases
|
Congenital Abnormality
|
64
|
27
|
0.030 |
None |
1.000 |
3 |
|
2017 |
2018 |
Periodontal Diseases
|
group |
Stomatognathic Diseases
|
Disease or Syndrome
|
326
|
22
|
0.020 |
None |
0.500 |
2 |
|
2015 |
2016 |
Latent Tuberculosis
|
disease |
Infections
|
Disease or Syndrome
|
183
|
18
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2019 |
Osteopenia
|
disease |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
845
|
61
|
0.020 |
None |
0.500 |
2 |
|
2018 |
2019 |
Tooth Loss
|
disease |
Stomatognathic Diseases
|
Acquired Abnormality
|
49
|
8
|
0.020 |
None |
0.500 |
2 |
|
2017 |
2019 |
Depressive Symptoms
|
phenotype |
Behavior and Behavior Mechanisms
|
Sign or Symptom
|
421
|
120
|
0.020 |
None |
1.000 |
2 |
|
2018 |
2019 |
Retinal defect
|
phenotype |
Eye Diseases
|
Anatomical Abnormality
|
13
|
|
0.020 |
None |
1.000 |
2 |
|
2006 |
2017 |
Infection - suppurative
|
group |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
20
|
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2018 |
Pallister-Hall syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
10
|
39
|
0.020 |
None |
1.000 |
2 |
|
1999 |
2012 |
Craniofacial Abnormalities
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
234
|
4
|
0.320 |
None |
1.000 |
2 |
|
2004 |
2012 |
Familial (FPAH)
|
disease |
|
Disease or Syndrome
|
1075
|
276
|
0.020 |
None |
1.000 |
2 |
|
1993 |
2007 |
Congenital hereditary endothelial dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
5
|
|
0.020 |
None |
1.000 |
2 |
|
2009 |
2016 |
Human immunodeficiency virus (HIV) II infection category B1
|
disease |
|
Disease or Syndrome
|
985
|
56
|
0.020 |
None |
1.000 |
2 |
|
2018 |
2019 |
Hypercholesterolemia, Familial
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
203
|
1423
|
0.020 |
None |
1.000 |
2 |
|
2004 |
2006 |
Hyperlipoproteinemia Type IIa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
201
|
661
|
0.020 |
None |
1.000 |
2 |
|
2004 |
2006 |