Preferred Name | inclusion body myositis | |
Synonyms |
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Definitions |
A myositis that is characterized by late onset of skeletal muscle inflammation, weakness, and atrophy with cytoplasmic granules and vacuoles in the muscle. OMIM mapping confirmed by DO. [SN]. |
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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_2023_03_01:72315009 UMLS_CUI:C0238190 ICD9CM:359.71 MESH:D018979 ICD10CM:G72.41 GARD:3896 MIM:147421 NCI:C84786 ORDO:611 |
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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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has exact match |
MESH:D018979 |
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has symptom | ||
has_obo_namespace |
disease_ontology |
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id |
DOID:3429 |
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in_subset |
http://purl.obolibrary.org/obo/doid#NCIthesaurus |
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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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subClassOf |
Create mapping