FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term anterior segment dysgenesis 3 ID (Ontology) DOID:0080608 (Human Disease)
Definition An anterior segment dysgenesis that has_material_basis_in heterozygous mutation in the FOXC1 gene on chromosome 6p25.
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
 anterior segment dysgenesis 3       1
 for disease ribbon | anterior segment dysgenesis 3       1
 model of | anterior segment dysgenesis 3       1
Spanning Tree (Parents/Children)
Only view relationship: 
monogenic disease
 |__anterior segment dysgenesis__
autosomal genetic disease        |
 |__autosomal dominant disease___|
eye disease                      |
 |__anterior segment dysgenesis__|
                                 anterior segment dysgenesis 3  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal dominant disease
anterior segment dysgenesis
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts
MIM:601631