FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term oculopharyngeal muscular dystrophy ID (Ontology) DOID:11719 (Human Disease)
Definition
Also Known As "Muscular dystrophy, oculopharyngeal"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS      28
Human Disease Models (FBhh)  DOID       1
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 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 oculopharyngeal muscular dystrophy      28     17      1
 ameliorates | oculopharyngeal muscular dystrophy      20       --       --
 exacerbates | oculopharyngeal muscular dystrophy       2       --       --
 for disease ribbon | oculopharyngeal muscular dystrophy       --       1       --
 model of | oculopharyngeal muscular dystrophy       6      1       --
Spanning Tree (Parents/Children)
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  myopathy
   |__muscular dystrophy
       |__oculopharyngeal muscular dystrophy  46 rec.
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Is a muscular dystrophy
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Synonyms
  • "Muscular dystrophy, oculopharyngeal" EXACT
Secondary IDs
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ICD10CM:G71.09
MESH:D039141
MIM:164300
NCI:C84942
SNOMEDCT_US_2023_03_01:77097004
UMLS_CUI:C0270952