loading...| Preferred Name |
Inclusion Body Myositis |
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| Synonyms |
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| Definitions |
An acquired or hereditary chronic inflammatory disorder of the muscles characterized by the morphologic finding of vacuoles and filamentous inclusions in the muscle tissues. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C84786 |
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| ALT_DEFINITION |
A rare form of progressive muscle disease that is notable for cytoplasmic granules and vacuoles in the muscle with little inflammation, and is usually refractory to treatment. Usually symptoms begin after the age of fifty. |
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| code |
C84786 |
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| Contributing_Source |
Cellosaurus NICHD |
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| definition |
An acquired or hereditary chronic inflammatory disorder of the muscles characterized by the morphologic finding of vacuoles and filamentous inclusions in the muscle tissues. |
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| in_subset |
http://purl.obolibrary.org/obo/NCIT_C90259 |
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| label |
Inclusion Body Myositis |
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| Preferred_Name |
Inclusion Body Myositis |
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| prefixIRI |
NCIT:C84786 |
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| prefLabel |
Inclusion Body Myositis |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0238190 |
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| subClassOf |