|
General Information
|
| Term |
patterned macular dystrophy 3 |
ID (Ontology) |
DOID:0060865 (Human Disease) |
| Definition |
A patterned macular dystrophy characterized by a 'dry desert land' pattern of the fundus, involving the posterior pole initially and progressing from the temporal fovea to the periphery of the retina developing in the fourth or fifth decade of life that has_material_basis_in heterozygous mutation in the MAPKAPK3 gene on chromosome 3p21. |
| Also Known As |
"Martinique crinkled retinal pigment epitheliopathy" ; "MDPT3" |
| 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 |
|---|
patterned macular dystrophy 3 | 1 | for disease ribbon | patterned macular dystrophy 3 | 1 | model of | patterned macular dystrophy 3 | 1 |
|
Relationships