FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term autosomal dominant centronuclear myopathy ID (Ontology) DOID:0111217 (Human Disease)
Definition A centronuclear myopathy that has_material_basis_in autosomal dominant inheritance.
Also Known As "AD-CNM"
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DO.org
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autosomal genetic disease
 |__autosomal dominant disease__
congenital structural myopathy  |
 |__centronuclear myopathy______|
                                autosomal dominant centronuclear myopathy  3 rec.
                                 |__centronuclear myopathy 1 3 rec.
                                 |__centronuclear myopathy 4
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Is a autosomal dominant disease
centronuclear myopathy
Part of
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Synonyms
  • "AD-CNM" EXACT OMO:0003012
Secondary IDs
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GARD:12719
ICD10CM:G71.228
MESH:D020914
ORDO:169189
SNOMEDCT_US_2023_03_01:716696006
UMLS_CUI:C1834558