macrophage activation syndrome |
Disease ID | 742 |
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Disease | macrophage activation syndrome |
Definition | A serious complication of childhood systemic inflammatory disorders that is thought to be caused by excessive activation and proliferation of T-LYMPHOCYTES and MACROPHAGES. It is seen predominantly in children with systemic onset JUVENILE IDIOPATHIC ARTHRITIS. |
Synonym | macrophage activation syndrome (disorder) macrophage activation syndrome [disease/finding] reactive hemophagocytic lymphohistiocytosis syndrome, macrophage activation |
Orphanet | |
UMLS | C1096155 |
MeSH | |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:33) C0553662 | juvenile idiopathic arthritis | 9 C0003864 | arthritis | 4 C0026691 | kawasaki disease | 4 C0024141 | systemic lupus erythematosus | 3 C0409974 | lupus erythematosus | 3 C0085273 | parvovirus b19 infection | 2 C0035435 | rheumatic disease | 2 C0019158 | hepatitis | 2 C0018203 | chronic granulomatous disease | 2 C0040034 | thrombocytopenia | 2 C0553662 | juvenile rheumatoid arthritis | 1 C0031039 | pericardial effusion | 1 C0009782 | connective tissue diseases | 1 C0021053 | immune disorder | 1 C0040188 | tic disorders | 1 C0002871 | anemia | 1 C0024291 | hemophagocytic lymphohistiocytosis | 1 C0021053 | immune disease | 1 C0085253 | adult-onset still's disease | 1 C0334121 | inflammatory myofibroblastic tumour | 1 C0041471 | typhus | 1 C0021053 | immune disorders | 1 C0085293 | hepatitis e | 1 C0023290 | visceral leishmaniasis | 1 C0021390 | inflammatory bowel disease | 1 C0011633 | dermatomyositis | 1 C0003873 | rheumatoid arthritis | 1 C0023484 | plasma cell leukemia | 1 C0009782 | connective tissue disease | 1 C0019348 | herpes simplex | 1 C0035435 | rheumatic diseases | 1 C0021831 | bowel disease | 1 C0036472 | scrub typhus | 1 |
Curated Gene | Entrez_id | Symbol | Resource(Total Genes:1) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | (Waiting for update.) |
Locus | (Waiting for update.) |
Disease ID | 742 |
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Disease | macrophage activation syndrome |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:20) HP:0005681 | Juvenile idiopathic arthritis | 8 HP:0001369 | Arthritis | 2 HP:0012115 | Liver inflammation | 2 HP:0002725 | Systemic lupus erythematosus | 2 HP:0001873 | Low platelet count | 2 HP:0002960 | Autoimmune condition | 2 HP:0100820 | Glomerulopathy | 1 HP:0100806 | Sepsis | 1 HP:0045073 | Serositis | 1 HP:0001903 | Anemia | 1 HP:0003281 | Increased ferritin | 1 HP:0001698 | Pericardial effusions | 1 HP:0002902 | Hyponatremia | 1 HP:0011900 | Hypofibrinogenemia | 1 HP:0100033 | Tic disorder | 1 HP:0006554 | Acute hepatic failure | 1 HP:0001399 | Liver failure | 1 HP:0001370 | Rheumatoid arthritis | 1 HP:0200119 | Acute liver inflammation | 1 HP:0002716 | Lymph node hyperplasia | 1 |
Disease ID | 742 |
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Disease | macrophage activation syndrome |
Manually Symptom | UMLS | Name(Total Manually Symptoms:1) C0948441 | vaso-occlusive disease |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:1) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
All Snps(Total Genotypes:1) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs104894176 | 23274377 | 5551 | PRF1 | umls:C1096155 | BeFree | Recurrent macrophage activation syndrome associated with heterozygous perforin W374X gene mutation in a child with systemic juvenile idiopathic arthritis. | 0.001085767 | 2013 | PRF1 | 10 | 70598599 | C | T |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Chemical(Total Drugs:0) | |
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(Waiting for update.) |
FDA approved drug and dosage information(Total Drugs:0) | |
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FDA labeling changes(Total Drugs:0) | |
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(Waiting for update.) |