FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term centronuclear myopathy X-linked ID (Ontology) DOID:0111225 (Human Disease)
Definition A centronuclear myopathy that has_material_basis_in X-linked inheritance of mutations in MTM1 on Xq28.
Also Known As "CNMX" ; "MTM1" ; "myotubular myopathy 1" (for all, see Synonyms field below)
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DO.org
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       1
Human Disease Models (FBhh)  DOID       1
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 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 centronuclear myopathy X-linked       1      1      1
 for disease ribbon | centronuclear myopathy X-linked       --       1       --
 model of | centronuclear myopathy X-linked       1      1       --
Spanning Tree (Parents/Children)
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  congenital structural myopathy
   |__centronuclear myopathy
       |__centronuclear myopathy X-linked  3 rec.
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Synonyms
  • "CNMX" EXACT OMO:0003012
    "MTM1" EXACT OMO:0003012
    "myotubular myopathy 1" EXACT
    "X-linked myotubular myopathy" EXACT
    "XLCNM" EXACT OMO:0003012
    "XLMTM" EXACT OMO:0003012
Secondary IDs
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GARD:11925
ICD10CM:G71.220
MESH:D020914
MIM:310400
NCI:C118781
ORDO:596
SNOMEDCT_US_2023_03_01:46804001
UMLS_CUI:C0410203