Corneal Dystrophy, Lattice Type IIIA
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
1
|
6
|
0.730 |
strong |
0.857 |
7 |
6
|
1998 |
2011 |
Groenouw corneal dystrophy type I (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
1
|
3
|
0.730 |
strong |
1.000 |
6 |
3
|
1998 |
2011 |
Corneal dystrophy, epithelial basement membrane
|
disease |
Eye Diseases; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
3
|
0.710 |
strong |
1.000 |
4 |
3
|
1998 |
2016 |
Epithelial basement membrane dystrophy
|
disease |
Eye Diseases; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
2
|
0.120 |
None |
0.500 |
2 |
2
|
2004 |
2016 |
Salzmann nodular dystrophy
|
disease |
Eye Diseases
|
Disease or Syndrome
|
1
|
1
|
0.010 |
None |
1.000 |
1 |
1
|
2009 |
2009 |
Nodular corneal dystrophy
|
phenotype |
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Punctate corneal dystrophy
|
disease |
|
Anatomical Abnormality
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Reis-Bucklers' corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
2
|
6
|
0.800 |
strong |
0.950 |
20 |
5
|
1998 |
2019 |
Thiel-behnke
|
disease |
|
Disease or Syndrome
|
2
|
2
|
0.030 |
None |
1.000 |
3 |
2
|
1999 |
2008 |
Hereditary corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
2
|
|
0.020 |
None |
1.000 |
2 |
|
1999 |
2005 |
Granulomatous iritis
|
disease |
Eye Diseases
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Corneal deposit
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
3
|
3
|
0.090 |
None |
1.000 |
9 |
3
|
1999 |
2018 |
Stromal Dystrophies, Corneal
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
3
|
1
|
0.020 |
None |
1.000 |
2 |
1
|
2000 |
2000 |
Visual impairment and blindness (excl colour blindness)
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Dystrophy, granular
|
disease |
|
Disease or Syndrome
|
4
|
8
|
0.050 |
None |
1.000 |
5 |
6
|
1995 |
2016 |
Amyloid of cornea
|
disease |
|
Disease or Syndrome
|
4
|
5
|
0.040 |
None |
0.750 |
4 |
3
|
2004 |
2007 |
Melorheostosis
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
4
|
2
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
4
|
23
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Macular corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
5
|
2
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Epithelial Recurrent Erosion Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
5
|
2
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Keratopathy
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
6
|
1
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Corneal guttata
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
6
|
1
|
0.010 |
None |
1.000 |
1 |
1
|
2000 |
2000 |
Schnyder crystalline corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
7
|
13
|
0.010 |
None |
1.000 |
1 |
1
|
2016 |
2016 |
Visual auras
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
7
|
1
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Familial Amyloid Polyneuropathy, Type V
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
8
|
19
|
0.200 |
None |
0.953 |
43 |
14
|
1999 |
2019 |