FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term polymicrogyria ID (Ontology) DOID:0080918 (Human Disease)
Definition A brain disease that is characterized by malformation of the developing brain characterized by abnormal cortical lamination and an unusual folding pattern of the cerebral cortex such that all or part of the brain surface is taken up by an excessive number of small folds (gyri).
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship:
  central nervous system disease
   |__brain disease
       |__polymicrogyria  3 rec.
           |__bilateral frontal polymicrogyria
           |__bilateral generalized polymicrogyria
           |__bilateral parasagittal parieto-occipital polymicrogyria 1 rec.
           |__bilateral perisylvian polymicrogyria 2 rec.
           |__unilateral focal polymicrogyria
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a brain disease
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts
MESH:D065706
NCI:C116936