FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term progressive myoclonus epilepsy ID (Ontology) DOID:891 (Human Disease)
Definition A variable age at onset electroclinical syndrome characterized by a relentlessly progressive disease course until death.
Also Known As "PME" ; "progressive myoclonic epilepsy"
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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       2
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
 Alleles Genes Human Disease Models
 progressive myoclonus epilepsy       2      1      1
 model of | progressive myoclonus epilepsy       2       --       --
Spanning Tree (Parents/Children)
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  electroclinical syndrome
   |__variable age at onset electroclinical syndrome
       |__progressive myoclonus epilepsy  19 rec.
           |__Lafora disease 4 rec.
           |__progressive myoclonus epilepsy 3
           |__progressive myoclonus epilepsy 4 3 rec.
           |__progressive myoclonus epilepsy 6 2 rec.
           |__progressive myoclonus epilepsy 7 1 rec.
           |__progressive myoclonus epilepsy 8
           |__progressive myoclonus epilepsy 9 2 rec.
           |__progressive myoclonus epilepsy 10 1 rec.
           |__Unverricht-Lundborg syndrome 3 rec.
               |__progressive myoclonus epilepsy 1A
               |__progressive myoclonus epilepsy 1B 3 rec.
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Is a variable age at onset electroclinical syndrome
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Synonyms
  • "PME" EXACT OMO:0003012
    "progressive myoclonic epilepsy" EXACT
Secondary IDs
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GARD:7140
MESH:D020191
MIM:310370
MIM:PS254800
NCI:C7636
SNOMEDCT_US_2023_03_01:192844008
UMLS_CUI:C0751778