Age-related cataract
|
disease |
Eye Diseases
|
Acquired Abnormality
|
92
|
15
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Cataract
|
disease |
Eye Diseases
|
Acquired Abnormality
|
878
|
124
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Superficial ulcer
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
242
|
10
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Impaired T cell function
|
phenotype |
|
Cell or Molecular Dysfunction
|
18
|
|
0.100 |
None |
|
0 |
|
|
|
Body mass index
|
phenotype |
|
Clinical Attribute
|
1014
|
2689
|
0.100 |
None |
1.000 |
1 |
1
|
2018 |
2018 |
Monosomy
|
group |
Pathological Conditions, Signs and Symptoms
|
Congenital Abnormality
|
214
|
11
|
0.040 |
None |
1.000 |
4 |
|
2000 |
2005 |
Congenital chromosomal disease
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
757
|
47
|
0.030 |
None |
1.000 |
3 |
|
1992 |
2009 |
Endocardial Cushion Defects
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
71
|
4
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Split hand foot deformity 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
71
|
8
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Anus, Imperforate
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
|
Congenital Abnormality
|
139
|
9
|
0.100 |
None |
|
0 |
|
|
|
Brachycephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
186
|
20
|
0.100 |
None |
|
0 |
|
|
|
Body mass index procedure
|
phenotype |
|
Diagnostic Procedure
|
88
|
252
|
0.100 |
None |
1.000 |
1 |
1
|
2013 |
2013 |
Cytokine Release Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Chemically-Induced Disorders
|
Disease or Syndrome
|
29
|
|
0.100 |
None |
0.920 |
25 |
|
2016 |
2020 |
Lupus Erythematosus, Systemic
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
1883
|
1172
|
0.100 |
None |
1.000 |
24 |
1
|
1998 |
2019 |
Craniosynostosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
488
|
90
|
0.100 |
None |
0.833 |
18 |
|
2017 |
2020 |
Autoimmune Diseases
|
group |
Immune System Diseases
|
Disease or Syndrome
|
1758
|
428
|
0.100 |
None |
0.938 |
16 |
|
1997 |
2019 |
Common Variable Immunodeficiency
|
disease |
Immune System Diseases
|
Disease or Syndrome
|
207
|
85
|
0.600 |
None |
1.000 |
16 |
|
2002 |
2020 |
Hypogammaglobulinemia
|
disease |
Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
76
|
2
|
0.570 |
strong |
0.750 |
8 |
|
1991 |
2019 |
B-cell aplasia
|
disease |
|
Disease or Syndrome
|
9
|
|
0.080 |
None |
1.000 |
8 |
|
2013 |
2020 |
Rheumatoid Arthritis
|
disease |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
|
Disease or Syndrome
|
2723
|
2387
|
0.070 |
None |
1.000 |
7 |
|
1996 |
2016 |
Immunologic Deficiency Syndromes
|
group |
Immune System Diseases
|
Disease or Syndrome
|
973
|
31
|
0.170 |
None |
1.000 |
7 |
|
1992 |
2013 |
Systemic Scleroderma
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
979
|
287
|
0.070 |
None |
0.857 |
7 |
2
|
2004 |
2018 |
Multiple Sclerosis
|
disease |
Immune System Diseases; Nervous System Diseases
|
Disease or Syndrome
|
1800
|
1022
|
0.060 |
None |
1.000 |
6 |
|
2003 |
2017 |
Severe Combined Immunodeficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases
|
Disease or Syndrome
|
284
|
46
|
0.060 |
None |
1.000 |
6 |
|
1992 |
1999 |
Graft-vs-Host Disease
|
disease |
Immune System Diseases
|
Disease or Syndrome
|
447
|
25
|
0.050 |
None |
1.000 |
5 |
|
2013 |
2019 |