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
Anemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
847
94
0.100
None
0
×
CUI:
C0015967
Disease:
Fever
Fever
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1021
66
0.100
None
0
Fibrinogen Deficiency
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Disease or Syndrome
56
4
0.100
None
0
Familial Hemophagocytic Lymphocytosis
phenotype
Hemic and Lymphatic Diseases
Disease or Syndrome
35
6
0.400
None
1.000
40
1
2001
2019
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
2
20
0.860
strong
1.000
28
20
2003
2019
Lymphohistiocytosis, Hemophagocytic
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
117
13
0.100
None
1.000
23
2003
2019
Familial (FPAH)
disease
Disease or Syndrome
1075
276
0.050
None
1.000
5
2006
2019
Macrophage Activation Syndrome
disease
Immune System Diseases
Disease or Syndrome
57
6
0.040
None
1.000
4
2008
2018
Systemic onset juvenile chronic arthritis
disease
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
Disease or Syndrome
90
53
0.040
None
1.000
4
2008
2018
Juvenile arthritis
disease
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
Disease or Syndrome
450
128
0.030
None
1.000
3
2008
2018
Arthritis
disease
Musculoskeletal Diseases
Disease or Syndrome
1072
69
0.010
None
1.000
1
2008
2008
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
Acute leukemia
disease
Pathological Conditions, Signs and Symptoms; Neoplasms
Neoplastic Process
639
50
0.010
None
1.000
1
2011
2011
Immune System Diseases
group
Immune System Diseases
Disease or Syndrome
451
116
0.010
None
1.000
1
2011
2011
Childhood Leukemia
disease
Neoplasms
Neoplastic Process
1740
140
0.010
None
1.000
1
2011
2011
Hydrops Fetalis
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
92
14
0.010
None
1.000
1
2011
2011
UNC13D Deficiency
disease
Immune System Diseases
Disease or Syndrome
2
0.010
None
1.000
1
2012
2012