Osteomyelitis
|
disease |
Infections; Musculoskeletal Diseases
|
Disease or Syndrome
|
121
|
14
|
0.020 |
None |
1.000 |
2 |
|
2020 |
2020 |
Gestational Diabetes
|
phenotype |
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
|
Disease or Syndrome
|
649
|
224
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Severe hereditary factor VIII deficiency disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
37
|
15
|
0.010 |
None |
1.000 |
1 |
1
|
2020 |
2020 |
Bronchopulmonary Dysplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
|
Disease or Syndrome
|
423
|
112
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
LACTASE PERSISTENCE
|
phenotype |
|
Disease or Syndrome
|
15
|
9
|
0.100 |
None |
0.978 |
45 |
|
1998 |
2019 |
Lactose Intolerance
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
11
|
2
|
0.200 |
None |
1.000 |
29 |
|
1991 |
2019 |
Lactose Intolerance, Adult Type
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
7
|
|
0.100 |
None |
1.000 |
15 |
|
2005 |
2019 |
Osteoporosis
|
disease |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
1098
|
182
|
0.030 |
None |
1.000 |
3 |
|
2004 |
2019 |
Diarrhea
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
632
|
63
|
0.130 |
None |
1.000 |
3 |
|
2018 |
2019 |
Lupus anticoagulant disorder
|
disease |
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
66
|
14
|
0.020 |
None |
1.000 |
2 |
|
2018 |
2019 |
Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
10161
|
1644
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Gingival Recession
|
disease |
Stomatognathic Diseases
|
Disease or Syndrome
|
14
|
1
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
White Blood Cell Count procedure
|
phenotype |
|
Laboratory Procedure
|
681
|
1322
|
0.100 |
None |
1.000 |
1 |
2
|
2019 |
2019 |
Adenomatous Polyposis Coli
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
609
|
237
|
0.010 |
None |
< 0.001 |
1 |
|
2019 |
2019 |
Lupus Vulgaris
|
disease |
Infections; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
526
|
44
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Oligospermia
|
disease |
Male Urogenital Diseases
|
Disease or Syndrome
|
217
|
72
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Lupus Erythematosus, Discoid
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
552
|
46
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Lupus Erythematosus, Systemic
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
1883
|
1172
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Xerocytosis
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
20
|
3
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Polycystic Ovary Syndrome
|
disease |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
|
Disease or Syndrome
|
988
|
363
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Recession
|
disease |
|
Anatomical Abnormality
|
13
|
2
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Impaired cognition
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
1630
|
348
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
74
|
68
|
0.010 |
None |
< 0.001 |
1 |
|
2019 |
2019 |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Stomatognathic Diseases
|
Disease or Syndrome
|
129
|
5
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Tumor Cell Invasion
|
phenotype |
|
Neoplastic Process
|
6626
|
169
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |