Muscular Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
280
|
67
|
0.200 |
None |
1.000 |
30 |
|
1996 |
2019 |
Epidermolysis Bullosa Simplex
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
30
|
33
|
0.300 |
None |
1.000 |
29 |
|
1991 |
2019 |
Epidermolysa bullosa simplex and limb girdle muscular dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
4
|
11
|
1.000 |
None |
1.000 |
23 |
11
|
1996 |
2017 |
Epidermolysis Bullosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
47
|
3
|
0.100 |
None |
1.000 |
20 |
|
1979 |
2019 |
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q
|
disease |
|
Disease or Syndrome
|
1
|
6
|
0.710 |
None |
1.000 |
9 |
6
|
1996 |
2017 |
Malignant Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
8621
|
1641
|
0.080 |
None |
1.000 |
8 |
|
2013 |
2018 |
Epidermolysis bullosa simplex, Ogna type
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
2
|
9
|
0.900 |
None |
1.000 |
8 |
7
|
1996 |
2013 |
Epidermolysis Bullosa Simplex With Pyloric Atresia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
2
|
9
|
0.730 |
None |
1.000 |
8 |
9
|
1996 |
2013 |
Pyloric Atresia
|
disease |
Digestive System Diseases
|
Congenital Abnormality
|
7
|
|
0.070 |
None |
1.000 |
7 |
|
2005 |
2017 |
Late-onset muscular dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
8
|
|
0.070 |
None |
1.000 |
7 |
|
1996 |
2013 |
Primary malignant neoplasm
|
group |
Neoplasms
|
Neoplastic Process
|
8221
|
1374
|
0.060 |
None |
1.000 |
6 |
|
2014 |
2018 |
Serum total cholesterol measurement
|
phenotype |
|
Laboratory Procedure
|
486
|
1243
|
0.100 |
None |
1.000 |
5 |
3
|
2010 |
2018 |
Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
10161
|
1644
|
0.050 |
None |
1.000 |
5 |
|
2013 |
2019 |
EPIDERMOLYSIS BULLOSA SIMPLEX WITH NAIL DYSTROPHY
|
disease |
|
Disease or Syndrome
|
1
|
6
|
0.400 |
None |
1.000 |
5 |
6
|
1996 |
2013 |
Low density lipoprotein cholesterol measurement
|
phenotype |
|
Laboratory Procedure
|
483
|
1142
|
0.100 |
None |
1.000 |
5 |
4
|
2010 |
2018 |
Tumor Cell Invasion
|
phenotype |
|
Neoplastic Process
|
6626
|
169
|
0.040 |
None |
1.000 |
4 |
|
2012 |
2019 |
Myasthenic Syndromes, Congenital
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
57
|
40
|
0.330 |
strong |
1.000 |
4 |
|
2011 |
2019 |
Neoplasm Metastasis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Neoplasms
|
Neoplastic Process
|
6385
|
327
|
0.040 |
None |
1.000 |
4 |
|
2013 |
2019 |
Pancreatic carcinoma
|
disease |
Digestive System Diseases; Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
2689
|
322
|
0.040 |
None |
1.000 |
4 |
|
2013 |
2018 |
Epidermolysis Bullosa Simplex Kobner
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
7
|
28
|
0.040 |
None |
1.000 |
4 |
1
|
2005 |
2017 |
Malignant neoplasm of pancreas
|
disease |
Digestive System Diseases; Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
2667
|
277
|
0.040 |
None |
1.000 |
4 |
|
2013 |
2018 |
Epidermolysis bullosa with pyloric atresia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
7
|
17
|
0.340 |
None |
1.000 |
4 |
|
2005 |
2016 |
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases
|
Disease or Syndrome
|
1410
|
80
|
0.040 |
None |
1.000 |
4 |
|
2013 |
2019 |
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
4
|
|
0.040 |
None |
1.000 |
4 |
|
1997 |
2016 |
Fibrinogen assay
|
phenotype |
|
Laboratory Procedure
|
55
|
143
|
0.100 |
None |
1.000 |
3 |
2
|
2013 |
2017 |