Agranulocytosis
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
55
8
0.100
None
0
Hypofibrinogenemia
disease
Disease or Syndrome
60
14
0.100
None
0
Reduced natural killer cell activity
phenotype
Finding
4
2
0.100
None
0
2
Unexplained fevers
phenotype
Pathological Conditions, Signs and Symptoms
Finding
14
4
0.100
None
0
2
Histiocytosis haematophagic
disease
Disease or Syndrome
36
2
0.100
None
0
2
Hypertriglyceridemia
phenotype
Nutritional and Metabolic Diseases
Disease or Syndrome
340
169
0.100
None
0
Hepatosplenomegaly
phenotype
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Hemic and Lymphatic Diseases
Sign or Symptom
127
21
0.100
None
0
Hepatomegaly
phenotype
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Finding
523
30
0.100
None
0
2
Fibrinogen Deficiency
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Disease or Syndrome
56
4
0.100
None
0
×
CUI:
C0015967
Disease:
Fever
Fever
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1021
66
0.100
None
0
Anemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
847
94
0.100
None
0
Increased susceptibility to malignancy
phenotype
Neoplasms
Finding
1
0.300
moderate
1.000
1
2014
2014
Malignant neoplasm of prostate
disease
Neoplasms; Male Urogenital Diseases
Neoplastic Process
4502
1082
0.300
None
1.000
1
2018
2018
Prostatic Neoplasms
group
Neoplasms; Male Urogenital Diseases
Neoplastic Process
1722
31
0.300
None
1.000
1
2018
2018
Major Depressive Disorder
disease
Mental Disorders
Mental or Behavioral Dysfunction
1236
1451
0.100
None
1.000
1
1
2017
2017
Cardiovascular Diseases
group
Cardiovascular Diseases
Disease or Syndrome
1756
711
0.100
None
1.000
1
1
2019
2019
Body mass index
phenotype
Clinical Attribute
1014
2689
0.100
None
1.000
1
1
2019
2019
Adult Lymphoma
disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
Neoplastic Process
1169
66
0.010
None
1.000
1
2019
2019
Childhood Leukemia
disease
Neoplasms
Neoplastic Process
1740
140
0.010
None
1.000
1
2011
2011
Childhood Lymphoma
disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
Neoplastic Process
1171
66
0.010
None
1.000
1
2019
2019
Neutrophil extracellular trap formation
disease
Disease or Syndrome
55
0.010
None
1.000
1
2012
2012
Cystinosis
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Disease or Syndrome
32
27
0.010
None
1.000
1
2019
2019
GRISCELLI SYNDROME, TYPE 2
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Immune System Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
4
11
0.010
None
1.000
1
2009
2009
UNC13D Deficiency
disease
Immune System Diseases
Disease or Syndrome
2
0.010
None
1.000
1
2012
2012
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
9
25
0.010
None
1.000
1
2017
2017