Acute leukemia
disease
Pathological Conditions, Signs and Symptoms; Neoplasms
Neoplastic Process
639
50
0.010
None
1.000
1
2011
2011
Adult Lymphoma
disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
Neoplastic Process
1169
66
0.010
None
1.000
1
2019
2019
Agranulocytosis
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
55
8
0.100
None
0
Anemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
847
94
0.100
None
0
Arthritis
disease
Musculoskeletal Diseases
Disease or Syndrome
1072
69
0.010
None
1.000
1
2008
2008
Autoimmune Lymphoproliferative Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
65
22
0.030
None
1.000
3
2013
2018
Body mass index
phenotype
Clinical Attribute
1014
2689
0.100
None
1.000
1
1
2019
2019
Breast Carcinoma
disease
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
6776
2793
0.010
None
1.000
1
2018
2018
Cardiovascular Diseases
group
Cardiovascular Diseases
Disease or Syndrome
1756
711
0.100
None
1.000
1
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
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
Dianzani autoimmune lymphoproliferative syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
7
0.010
None
1.000
1
2013
2013
Epstein-Barr Virus Infections
group
Infections
Disease or Syndrome
384
72
0.020
None
1.000
2
2014
2015
Exanthema
phenotype
Skin and Connective Tissue Diseases
Sign or Symptom
251
14
0.010
None
1.000
1
2019
2019
Familial (FPAH)
disease
Disease or Syndrome
1075
276
0.050
None
1.000
5
2006
2019
Familial Hemophagocytic Lymphocytosis
phenotype
Hemic and Lymphatic Diseases
Disease or Syndrome
35
6
0.400
None
1.000
40
1
2001
2019
×
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
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
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
9
25
0.010
None
1.000
1
2017
2017
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
2
20
0.860
strong
1.000
28
20
2003
2019
Hepatomegaly
phenotype
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Finding
523
30
0.100
None
0
2
Hepatosplenomegaly
phenotype
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Hemic and Lymphatic Diseases
Sign or Symptom
127
21
0.100
None
0
Histiocytosis haematophagic
disease
Disease or Syndrome
36
2
0.100
None
0
2