|
General Information
|
| Term |
anterior segment dysgenesis 2 |
ID (Ontology) |
DOID:0080607 (Human Disease) |
| Definition |
An anterior segment dysgenesis that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the FOXE3 gene on chromosome 1p33. |
| Comment |
|
|
Links to External Ontologies
|
|
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)
|
|
No relevant records available
|
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 2 | 3 | for disease ribbon | anterior segment dysgenesis 2 | 3 | model of | anterior segment dysgenesis 2 | 3 |
|