Multiple Sclerosis
|
disease |
Immune System Diseases; Nervous System Diseases
|
Disease or Syndrome
|
1800
|
1022
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |
Osteoporosis
|
disease |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
1098
|
182
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Periodontitis
|
disease |
Stomatognathic Diseases
|
Disease or Syndrome
|
682
|
116
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Pneumothorax
|
phenotype |
Respiratory Tract Diseases
|
Disease or Syndrome
|
69
|
3
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Pulmonary Emphysema
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
352
|
64
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Ureteral obstruction
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
359
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Epidermolysis Bullosa Dystrophica
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
15
|
15
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Hallopeau-Siemens Disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
51
|
54
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Iron-Refractory Iron Deficiency Anemia
|
disease |
Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
51
|
36
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Osteoid formation disorder
|
disease |
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Fibrosis, Liver
|
disease |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Disease or Syndrome
|
1179
|
64
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Gastroschisis
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
31
|
8
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Osteogenesis imperfecta type III (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
18
|
67
|
0.300 |
None |
1.000 |
1 |
|
2012 |
2012 |
Coinfection
|
phenotype |
Infections
|
Disease or Syndrome
|
252
|
11
|
0.010 |
None |
1.000 |
1 |
|
2003 |
2003 |
Chronic liver disease
|
group |
Digestive System Diseases
|
Disease or Syndrome
|
196
|
14
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Cholesteryl Ester Transfer Protein Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
22
|
5
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Protein C Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
43
|
14
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Specific language impairment
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
34
|
9
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Hypoalphalipoproteinemias
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
20
|
7
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
hiv-infection/aids
|
disease |
Infections
|
Disease or Syndrome
|
124
|
4
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Factor V Leiden mutation
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
86
|
46
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Pneumocystis Infections
|
group |
Infections
|
Disease or Syndrome
|
18
|
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Coronary Artery Disease
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1708
|
1577
|
0.100 |
None |
1.000 |
1 |
2
|
2018 |
2018 |
HIV-1 infection
|
disease |
|
Disease or Syndrome
|
695
|
94
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
OSTEOGENESIS IMPERFECTA, TYPE XII
|
disease |
|
Disease or Syndrome
|
3
|
5
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |