(non-specific) purulent meningitis
|
disease |
|
Disease or Syndrome
|
6
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
AA amyloidosis
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
38
|
10
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2018 |
Abdominal Abscess
|
disease |
Infections
|
Disease or Syndrome
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Abdominal Pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
302
|
18
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Abdominal symptom
|
phenotype |
|
Sign or Symptom
|
17
|
3
|
0.020 |
None |
1.000 |
2 |
|
2012 |
2015 |
ABLEPHARON-MACROSTOMIA SYNDROME
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Stomatognathic Diseases
|
Disease or Syndrome
|
41
|
14
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Abnormal behavior
|
phenotype |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
910
|
121
|
0.080 |
None |
0.875 |
8 |
1
|
2017 |
2019 |
Abnormality of limbs
|
phenotype |
|
Anatomical Abnormality
|
8
|
1
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |
ABO incompatibility
|
disease |
Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
14
|
2
|
0.020 |
None |
1.000 |
2 |
|
1991 |
1994 |
Abscess
|
phenotype |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
96
|
1
|
0.020 |
None |
1.000 |
2 |
|
2007 |
2020 |
Absence of sensation
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
111
|
5
|
0.020 |
None |
1.000 |
2 |
|
2003 |
2018 |
Acanthosis Nigricans
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
64
|
11
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Achalasia
|
disease |
|
Disease or Syndrome
|
40
|
5
|
0.020 |
None |
0.500 |
2 |
1
|
2014 |
2018 |
CUI: |
C0234238 |
Disease: |
Ache
|
Ache
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
50
|
|
0.300 |
None |
1.000 |
2 |
|
2008 |
2010 |
Achondroplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
46
|
21
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Acidosis, Lactic
|
phenotype |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
209
|
21
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
CUI: |
C0702166 |
Disease: |
Acne
|
Acne
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
167
|
11
|
0.060 |
None |
1.000 |
6 |
|
2010 |
2016 |
Acne Vulgaris
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
94
|
37
|
0.060 |
None |
1.000 |
6 |
|
2010 |
2016 |
Acoustic Neuroma
|
disease |
Neoplasms; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Neoplastic Process
|
131
|
3
|
0.020 |
None |
1.000 |
2 |
|
2015 |
2017 |
Acquired aplastic anemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
64
|
12
|
0.020 |
None |
1.000 |
2 |
|
2015 |
2018 |
Acquired hallux valgus
|
disease |
Musculoskeletal Diseases
|
Acquired Abnormality
|
14
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Acquired Hypogammaglobulinemia
|
disease |
Immune System Diseases
|
Disease or Syndrome
|
89
|
4
|
0.020 |
None |
0.500 |
2 |
|
1997 |
2001 |
Acquired Immunodeficiency Syndrome
|
group |
Infections; Immune System Diseases
|
Disease or Syndrome
|
243
|
42
|
0.200 |
None |
0.909 |
11 |
2
|
1992 |
2020 |
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
|
phenotype |
|
Finding
|
147
|
526
|
0.100 |
None |
1.000 |
2 |
3
|
2009 |
2010 |
Acro-Osteolysis
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
16
|
1
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |