FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term anencephaly ID (Ontology) DOID:0060668 (Human Disease)
Definition A congenital nervous system abnormality characterized by failure of the anterior neuropore to close resulting in partial or complete absence of the cranial vault accompanied by absence of overlying tissues, including the brain and cerebral hemispheres, skull and scalp.
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
 Full annotation statements 
Relevant FlyBase reports
 Genes
 anencephaly       1
 for disease ribbon | anencephaly       1
 model of | anencephaly       1
Spanning Tree (Parents/Children)
Only view relationship: 
physical disorder_______
nervous system disease__|
                        congenital nervous system abnormality
                         |__anencephaly  1 rec.
                             |__hydranencephaly
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a congenital nervous system abnormality
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts
GARD:5808
ICD10CM:Q00.0
MESH:D000757
MIM:206500
ORDO:1048