Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
|
disease |
|
Disease or Syndrome
|
593
|
24
|
0.020 |
None |
1.000 |
2 |
|
2008 |
2016 |
Tumor Cell Invasion
|
phenotype |
|
Neoplastic Process
|
6626
|
169
|
0.020 |
None |
1.000 |
2 |
|
2004 |
2019 |
Malignant neoplasm of colon and/or rectum
|
disease |
|
Neoplastic Process
|
3669
|
502
|
0.020 |
None |
1.000 |
2 |
|
2003 |
2007 |
Morphologically abnormal structure (morphologic abnormality)
|
group |
|
Anatomical Abnormality
|
20
|
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Global developmental delay
|
disease |
|
Mental or Behavioral Dysfunction
|
1825
|
553
|
0.010 |
None |
1.000 |
1 |
|
1980 |
1980 |
Limb defects
|
group |
|
Congenital Abnormality
|
67
|
2
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Corneal calcification
|
phenotype |
|
Anatomical Abnormality
|
10
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Tonic clonic movements
|
disease |
|
Disease or Syndrome
|
22
|
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Differentiated Thyroid Gland Carcinoma
|
disease |
|
Neoplastic Process
|
245
|
80
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Serum total cholesterol measurement
|
phenotype |
|
Laboratory Procedure
|
486
|
1243
|
0.100 |
None |
1.000 |
1 |
1
|
2018 |
2018 |
B-CELL MALIGNANCY, LOW-GRADE
|
disease |
|
Neoplastic Process
|
350
|
19
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |
Avascular retina
|
disease |
|
Disease or Syndrome
|
19
|
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Congenital Abnormality
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
1098
|
73
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Wolf-Hirschhorn Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Disease or Syndrome
|
34
|
2
|
0.010 |
None |
1.000 |
1 |
|
2003 |
2003 |
Adenomatous Polyposis Coli
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
609
|
237
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Cystic Fibrosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases
|
Disease or Syndrome
|
852
|
704
|
0.010 |
None |
1.000 |
1 |
|
1990 |
1990 |
Retinopathy of Prematurity
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
202
|
16
|
0.030 |
None |
1.000 |
3 |
|
2011 |
2020 |
Congenital neutropenia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Congenital Abnormality
|
68
|
11
|
0.020 |
None |
1.000 |
2 |
|
2007 |
2009 |
Severe congenital neutropenia
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
66
|
26
|
0.020 |
None |
1.000 |
2 |
|
2007 |
2009 |
LIMB-MAMMARY SYNDROME
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
120
|
1
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Familial multiple trichoepitheliomata
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
317
|
32
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Hereditary Melanoma
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
50
|
67
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Bronchopulmonary Dysplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
|
Disease or Syndrome
|
423
|
112
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Ulcerative Colitis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
1458
|
827
|
0.010 |
None |
< 0.001 |
1 |
|
2007 |
2007 |
Gastritis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
292
|
21
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |