Tumor Cell Invasion
|
phenotype |
|
Neoplastic Process
|
6626
|
169
|
0.100 |
None |
1.000 |
13 |
|
2007 |
2019 |
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 |
Thiel-behnke
|
disease |
|
Disease or Syndrome
|
2
|
2
|
0.030 |
None |
1.000 |
3 |
2
|
1999 |
2008 |
Familial (FPAH)
|
disease |
|
Disease or Syndrome
|
1075
|
276
|
0.020 |
None |
1.000 |
2 |
1
|
2008 |
2009 |
Adult Erythroleukemia
|
disease |
|
Neoplastic Process
|
236
|
4
|
0.020 |
None |
1.000 |
2 |
|
1990 |
1991 |
Myelodysplasia
|
disease |
|
Congenital Abnormality
|
135
|
3
|
0.010 |
None |
1.000 |
1 |
|
1994 |
1994 |
Nodule
|
phenotype |
|
Acquired Abnormality
|
278
|
19
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Hypocupremia
|
disease |
|
Disease or Syndrome
|
21
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
CUI: |
C0860659 |
Disease: |
Aloof
|
Aloof
|
disease |
|
Mental or Behavioral Dysfunction
|
81
|
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Vascular lesions
|
disease |
|
Disease or Syndrome
|
111
|
9
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
tumor vasculature
|
phenotype |
|
Neoplastic Process
|
200
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Clinically isolated syndrome
|
disease |
|
Disease or Syndrome
|
54
|
2
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
CUI: |
C4699184 |
Disease: |
Fuchs
|
Fuchs
|
disease |
|
Disease or Syndrome
|
10
|
5
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
HER2-negative breast cancer
|
disease |
|
Neoplastic Process
|
160
|
18
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Depressed mood
|
phenotype |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
1459
|
269
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Heart Diseases
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
476
|
44
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
44
|
20
|
0.200 |
None |
0.992 |
117 |
7
|
1996 |
2019 |
Lattice corneal dystrophy Type I
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
11
|
12
|
0.800 |
strong |
0.960 |
45 |
10
|
1998 |
2019 |
Avellino corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
114
|
14
|
0.800 |
strong |
1.000 |
38 |
5
|
1998 |
2019 |
Granular Dystrophy, Corneal
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
7
|
6
|
0.200 |
None |
0.964 |
28 |
5
|
1994 |
2018 |
Reis-Bucklers' corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
2
|
6
|
0.800 |
strong |
0.950 |
17 |
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 |
5 |
4
|
1998 |
2015 |
Fuchs Endothelial Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
90
|
25
|
0.040 |
None |
1.000 |
4 |
|
1996 |
2019 |
Groenouw corneal dystrophy type I (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
1
|
2
|
0.730 |
strong |
1.000 |
3 |
2
|
1998 |
2011 |