FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term inclusion body myositis ID (Ontology) DOID:3429 (Human Disease)
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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DO.org
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       3
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 Alleles Genes
 inclusion body myositis       3      3
 ameliorates | inclusion body myositis       1       --
 model of | inclusion body myositis       2       --
Spanning Tree (Parents/Children)
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  myopathy
   |__myositis
       |__inclusion body myositis  6 rec.
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Synonyms
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GARD:3896
ICD10CM:G72.41
ICD9CM:359.71
MESH:D018979
MIM:147421
NCI:C84786
ORDO:611
SNOMEDCT_US_2023_03_01:72315009
UMLS_CUI:C0238190