Lattice corneal dystrophy Type I
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
11
|
13
|
0.800 |
strong |
0.960 |
50 |
11
|
1998 |
2019 |
Avellino corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
115
|
14
|
0.800 |
strong |
1.000 |
40 |
5
|
1998 |
2019 |
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 corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
12
|
4
|
0.750 |
strong |
1.000 |
7 |
4
|
1998 |
2015 |
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 |
Diabetic Nephropathy
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
1189
|
238
|
0.530 |
None |
1.000 |
4 |
|
2003 |
2012 |
Sepsis
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
1453
|
144
|
0.330 |
None |
1.000 |
3 |
|
2017 |
2020 |
Septicemia
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
1285
|
141
|
0.330 |
None |
1.000 |
3 |
|
2017 |
2020 |
Severe Sepsis
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
181
|
29
|
0.300 |
None |
1.000 |
1 |
|
2017 |
2017 |
Spontaneous abortion
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
188
|
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Nodular glomerulosclerosis
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
59
|
|
0.300 |
None |
1.000 |
1 |
|
2009 |
2009 |
Pyemia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Infections
|
Pathologic Function
|
24
|
|
0.300 |
None |
1.000 |
1 |
|
2017 |
2017 |
Miscarriage
|
disease |
Female Urogenital Diseases and Pregnancy Complications
|
Disease or Syndrome
|
426
|
56
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Abortion, Tubal
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
109
|
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Early Pregnancy Loss
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Finding
|
109
|
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Kidney Diseases
|
group |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
1180
|
140
|
0.210 |
None |
1.000 |
2 |
|
2001 |
2006 |
Corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
113
|
25
|
0.200 |
None |
0.992 |
123 |
8
|
1996 |
2019 |
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 |
Granular Dystrophy, Corneal
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
8
|
6
|
0.200 |
None |
0.964 |
28 |
5
|
1994 |
2018 |
Tubulointerstitial fibrosis
|
phenotype |
|
Disease or Syndrome
|
328
|
|
0.200 |
None |
1.000 |
1 |
|
2004 |
2004 |
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 |
Cataract
|
disease |
Eye Diseases
|
Acquired Abnormality
|
878
|
124
|
0.120 |
None |
1.000 |
2 |
|
2000 |
2002 |
Recurrent erosion of cornea
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases
|
Disease or Syndrome
|
15
|
|
0.110 |
None |
1.000 |
1 |
|
1999 |
1999 |