×
CUI:
C0030193
Disease:
Pain
Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1554
196
0.010
None
1.000
1
2019
2019
Vomiting
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
303
23
0.010
None
1.000
1
2018
2018
Abdominal Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
302
18
0.100
None
0
Hemorrhage
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
47
0.300
strong
1.000
1
1998
1998
Epistaxis
phenotype
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
Pathologic Function
82
4
0.100
None
0
Gingival Hemorrhage
phenotype
Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases
Pathologic Function
50
2
0.100
None
0
Colorectal Carcinoma
disease
Digestive System Diseases; Neoplasms
Neoplastic Process
5473
1962
0.020
None
1.000
2
2011
2017
Malignant neoplasm of breast
disease
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
6941
3417
0.010
None
1.000
1
2018
2018
Leukemia, Myelocytic, Acute
disease
Neoplasms
Neoplastic Process
3111
6892
0.100
None
1.000
1
2
2017
2017
Breast Carcinoma
disease
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
6776
2793
0.010
None
1.000
1
2018
2018
Melanocytic nevus
disease
Neoplasms
Neoplastic Process
297
33
0.100
None
0
Schizophrenia
disease
Mental Disorders
Mental or Behavioral Dysfunction
2872
2897
0.010
None
1.000
1
2013
2013
Serum albumin measurement
phenotype
Laboratory Procedure
433
3282
0.100
None
1.000
1
15
2013
2013
Freckles
phenotype
Skin and Connective Tissue Diseases
Finding
45
10
0.100
None
0
Prolonged bleeding time
phenotype
Finding
39
3
0.100
None
0
Increased tendency to bruise
phenotype
Wounds and Injuries
Finding
133
14
0.100
None
0
Freckles in sun-exposed areas
phenotype
Finding
5
1
0.100
None
0
Nystagmus, CTCAE 3.0
phenotype
Finding
779
0.100
None
0
Restrictive ventilatory defect
phenotype
Finding
61
8
0.100
None
0
Nystagmus, CTCAE 5.0
phenotype
Finding
779
0.100
None
0
Hantavirus Infections
group
Infections
Disease or Syndrome
108
10
0.100
None
1.000
34
1
1997
2019
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
9
9
0.940
definitive
1.000
33
8
1978
2018
Hermanski-Pudlak Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
70
59
0.500
None
1.000
32
22
1996
2019
Platelet Storage Pool Deficiency
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
22
1
0.210
None
1.000
13
1978
2008
Pulmonary Fibrosis
disease
Respiratory Tract Diseases
Disease or Syndrome
924
25
0.480
strong
0.889
9
1998
2019