FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term visceral heterotaxy 1 ID (Ontology) DOID:0051016 (Human Disease)
Definition A visceral heterotaxy that is characterized by randomization of the placement of visceral organs, including the heart, lungs, liver, spleen, and stomach and that has_material_basis_in mutation in the ZIC3 gene on chromosome Xq26.
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
 visceral heterotaxy 1       1
 for disease ribbon | visceral heterotaxy 1       1
 model of | visceral heterotaxy 1       1
Spanning Tree (Parents/Children)
Only view relationship:
X-linked monogenic disease
 |__X-linked recessive disease__
physical disorder               |
 |__visceral heterotaxy_________|
                                visceral heterotaxy 1  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a visceral heterotaxy
X-linked recessive disease
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts
MIM:306955