Larva Migrans, Cutaneous
disease
Infections; Skin and Connective Tissue Diseases
Disease or Syndrome
1
0.010
None
1.000
1
2018
2018
Prekallikrein deficiency
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
5
6
0.010
None
1.000
1
1986
1986
Disorientation
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
Sign or Symptom
12
0.010
None
1.000
1
2018
2018
Hemodynamic instability
disease
Disease or Syndrome
15
0.010
None
1.000
1
2018
2018
Enteritis due to Norovirus
disease
Infections
Disease or Syndrome
16
0.010
None
1.000
1
2018
2018
Bacteremia due to Staphylococcus aureus
disease
Pathological Conditions, Signs and Symptoms; Infections
Disease or Syndrome
17
1
0.010
None
1.000
1
2017
2017
Infection caused by Norovirus
group
Infections
Disease or Syndrome
18
0.010
None
1.000
1
2018
2018
Intestinal Diseases, Parasitic
group
Digestive System Diseases; Infections
Disease or Syndrome
19
0.010
None
1.000
1
2018
2018
×
CUI:
C0205204
Disease:
Scab
Scab
disease
Acquired Abnormality
24
0.010
None
1.000
1
2017
2017
Marijuana Use
disease
Mental Disorders; Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
33
0.010
None
1.000
1
2018
2018
Hermaphroditism
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
Disease or Syndrome
34
0.010
None
1.000
1
2018
2018
Gray Platelet Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Disease or Syndrome
38
14
0.010
None
1.000
1
2018
2018
Pseudocholinesterase Measurement
phenotype
Laboratory Procedure
39
568
0.100
None
1.000
1
20
2011
2011
Cerebral hypoperfusion
disease
Disease or Syndrome
40
1
0.010
None
1.000
1
2020
2020
Chediak-Higashi Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
41
14
0.010
None
1.000
1
2014
2014
Severe diarrhea
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
47
6
0.010
None
1.000
1
2011
2011
Pressure Ulcer
disease
Skin and Connective Tissue Diseases
Disease or Syndrome
49
1
0.010
None
1.000
1
2017
2017
Hemophilia B
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Disease or Syndrome
59
125
0.010
None
1.000
1
1985
1985
Helminthiasis
disease
Infections
Disease or Syndrome
59
1
0.010
None
1.000
1
2018
2018
Melioidosis
disease
Infections
Disease or Syndrome
65
9
0.010
None
1.000
1
2018
2018
Vegetation
disease
Anatomical Abnormality
67
0.020
None
1.000
2
2017
2019
Systemic candidiasis
disease
Infections
Disease or Syndrome
73
0.010
None
1.000
1
2001
2001
Skin Diseases, Infectious
group
Infections; Skin and Connective Tissue Diseases
Disease or Syndrome
74
0.010
None
1.000
1
2018
2018
Confusion
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
75
5
0.010
None
1.000
1
2018
2018
psychological distress
disease
Mental or Behavioral Dysfunction
87
10
0.010
None
1.000
1
2017
2017