eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| idiopathic inflammatory myopathy | ||||
| Disease ID | 1706 |
|---|---|
| Disease | idiopathic inflammatory myopathy |
| Definition | An umbrella term for diseases which have chronic muscle inflammation and weakness of unknown etiology. The types of idiopathic inflammatory myopathy are further defined by either clinicopathologic criteria or by the presence of certain autoantibodies. |
| Synonym | idiopathic inflamm myopathies idiopathic inflammatory myopathies idiopathic inflammatory myopathy (disorder) idiopathic inflammatory myositis iim inflamm myopathies idiopathic inflammatory myopathies, idiopathic inflammatory myopathy, idiopathic myopathies idiopathic inflamm myopathies, idiopathic inflammatory myopathy, idiopathic inflammatory |
| Orphanet | |
| OMIM | |
| UMLS | C0751356 |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:10) C0206062 | interstitial lung disease | 5 C0024115 | lung disease | 5 C0027121 | myositis | 2 C0003864 | arthritis | 1 C0032285 | pneumonia | 1 C0021053 | immune disorder | 1 C0010068 | coronary artery disease | 1 C0011633 | dermatomyositis | 1 C0026848 | muscle disease | 1 C0042721 | viral hepatitis | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | Entrez_id | Symbol | Resource(Total Genes:4) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1706 |
|---|---|
| Disease | idiopathic inflammatory myopathy |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:12) HP:0006530 | Interstitial lung disease | 5 HP:0100614 | Muscle inflammation | 2 HP:0002721 | Immunodeficiency | 1 HP:0004349 | Reduced bone mineral density | 1 HP:0002090 | Pneumonia | 1 HP:0006562 | Viral hepatitis | 1 HP:0002910 | Elevated transaminases | 1 HP:0001677 | Coronary artery disease | 1 HP:0001907 | Thromboembolic disease | 1 HP:0005952 | Decreased lung function | 1 HP:0001369 | Arthritis | 1 HP:0001324 | Muscular weakness | 1 |
| Disease ID | 1706 |
|---|---|
| Disease | idiopathic inflammatory myopathy |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:1) C2364118 | weakness |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:1) |
Manually Genotype(Total Text Mining Genotypes:0) |
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| (Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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| (Waiting for update.) | |
All Snps(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
|---|---|
| (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.) |
| Disease ID | 1706 |
|---|---|
| Disease | idiopathic inflammatory myopathy |
| Case | (Waiting for update.) |