FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term chronic progressive external ophthalmoplegia ID (Ontology) DOID:12558 (Human Disease)
Definition
Also Known As "progressive external ophthalmoplegia"
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
Human Disease Models (FBhh)  DOID       1
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Human Disease Models
 chronic progressive external ophthalmoplegia       1
Spanning Tree (Parents/Children)
Only view relationship: 
  myopathy
   |__mitochondrial myopathy
       |__chronic progressive external ophthalmoplegia  24 rec.
           |__autosomal dominant progressive external ophthalmoplegia 1 2 rec.
           |__autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 2 rec.
           |__autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 8 rec.
           |__autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 6 rec.
           |__autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5 3 rec.
           |__autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 1 rec.
           |__autosomal recessive progressive external ophthalmoplegia 1 2 rec.
           |__autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2 1 rec.
           |__autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3 1 rec.
           |__autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4 1 rec.
           |__autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5 1 rec.
           |__Kearns-Sayre syndrome
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a mitochondrial myopathy
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "progressive external ophthalmoplegia" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:4503
ICD10CM:H49.4
ICD9CM:378.72
MESH:D017246
MIM:PS157640
SNOMEDCT_US_2023_03_01:194126004
UMLS_CUI:C0162674