Fatigue
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
760
|
67
|
0.100 |
None |
|
0 |
|
|
|
Blood Coagulation Disorders
|
group |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
267
|
31
|
0.100 |
None |
|
0 |
|
|
|
Increased serum ferritin
|
phenotype |
|
Finding
|
23
|
1
|
0.100 |
None |
|
0 |
|
|
|
Histiocytosis haematophagic
|
disease |
|
Disease or Syndrome
|
36
|
2
|
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 |
|
|
|
CUI: |
C0015967 |
Disease: |
Fever
|
Fever
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
1021
|
66
|
0.100 |
None |
|
0 |
|
|
|
Variable expressivity
|
phenotype |
|
Finding
|
319
|
|
0.100 |
None |
|
0 |
|
|
|
Erythematous plaque
|
phenotype |
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Weight decreased
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
271
|
3
|
0.100 |
None |
|
0 |
|
|
|
Hypertriglyceridemia
|
phenotype |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
340
|
169
|
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 |
|
|
|
Hypofibrinogenemia
|
disease |
|
Disease or Syndrome
|
60
|
14
|
0.100 |
None |
|
0 |
|
|
|
Skin Ulcer
|
phenotype |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
151
|
1
|
0.100 |
None |
|
0 |
|
|
|
Erythematous papule
|
phenotype |
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Chills
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
34
|
|
0.100 |
None |
|
0 |
|
|
|
Lymphohistiocytosis, Hemophagocytic
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
117
|
13
|
0.310 |
None |
1.000 |
1 |
|
2018 |
2018 |
Familial Hemophagocytic Lymphocytosis
|
phenotype |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
35
|
6
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Reactive Hemophagocytic Syndrome
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Hemophagocytic Lymphohistiocytosis, Familial, 1
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
5
|
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Hemophagocytic Syndrome
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
25
|
3
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Neuritis, Autoimmune, Experimental
|
disease |
Immune System Diseases; Nervous System Diseases
|
Experimental Model of Disease
|
32
|
|
0.200 |
None |
1.000 |
1 |
|
2011 |
2011 |
Graft Rejection
|
phenotype |
|
Organ or Tissue Function
|
47
|
|
0.200 |
None |
1.000 |
1 |
|
2014 |
2014 |
Transient Ischemic Attack
|
disease |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
344
|
16
|
0.200 |
None |
1.000 |
1 |
|
2015 |
2015 |
Experimental Autoimmune Encephalomyelitis
|
disease |
Immune System Diseases; Nervous System Diseases
|
Experimental Model of Disease
|
97
|
|
0.200 |
None |
1.000 |
1 |
|
2005 |
2005 |
Panniculitis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
37
|
2
|
0.110 |
None |
1.000 |
1 |
|
2000 |
2000 |