loading...| Preferred Name |
inclusion body myositis |
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| Synonyms |
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| Definitions |
OMIM mapping confirmed by DO. [SN]. A myositis that is characterized by late onset of skeletal muscle inflammation, weakness, and atrophy with cytoplasmic granules and vacuoles in the muscle. |
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| ID |
http://purl.obolibrary.org/obo/DOID_3429 |
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| comment |
OMIM mapping confirmed by DO. [SN]. |
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| database_cross_reference |
SNOMEDCT_US_2020_03_01:72315009 UMLS_CUI:C0238190 OMIM:147421 ICD9CM:359.71 MESH:D018979 ICD10CM:G72.41 GARD:3896 NCI:C84786 ORDO:611 |
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| has exact match |
MESH:D018979 |
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| has_obo_namespace |
disease_ontology |
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| id |
DOID:3429 |
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| imported from | ||
| in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/doid#NCIthesaurus http://purl.oboInOwllibrary.org/oboInOwl/doid#DO_FlyBase_slim |
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| label |
inclusion body myositis |
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| notation |
DOID:3429 |
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| prefLabel |
inclusion body myositis |
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| textual definition |
A myositis that is characterized by late onset of skeletal muscle inflammation, weakness, and atrophy with cytoplasmic granules and vacuoles in the muscle. |
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| subClassOf |
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