|
General Information
|
| Term |
retinal macular dystrophy 4 |
ID (Ontology) |
DOID:0070441 (Human Disease) |
| Definition |
A retinal macular dystrophy characterized by late-onset macular degeneration, with multiple drusen-like deposits, macular geographic atrophy, and choroidal neovascularization that has_material_basis_in heterozygous mutation in the CLEC3B gene on chromosome 3p21. |
| Also Known As |
"MCDR4" |
| 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 |
|---|
retinal macular dystrophy 4 | 3 | for disease ribbon | retinal macular dystrophy 4 | 3 | model of | retinal macular dystrophy 4 | 3 |
|