FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term centronuclear myopathy 2 ID (Ontology) DOID:0111220 (Human Disease)
Definition An autosomal recessive centronuclear myopathy that has_material_basis_in homozygous or compound heterozygous mutation in BIN1 on 2q14.3.
Also Known As "CNM2"
Comment
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DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       2
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 centronuclear myopathy 2       2      1      1
 for disease ribbon | centronuclear myopathy 2       --       1       --
 model of | centronuclear myopathy 2       2      1       --
Spanning Tree (Parents/Children)
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autosomal recessive disease__
centronuclear myopathy_______|
                             autosomal recessive centronuclear myopathy
                              |__centronuclear myopathy 2  4 rec.
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Is a autosomal recessive centronuclear myopathy
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Synonyms
  • "CNM2" EXACT OMO:0003012
Secondary IDs
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MESH:C562934
MIM:255200
SNOMEDCT_US_2023_03_01:240081004
UMLS_CUI:C0410204