|
| General Information | |||
|---|---|---|---|
| Term | basal laminar drusen | ID (Ontology) | DOID:0060746 (Human Disease) |
| Definition | A retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium on Bruch membrane and that has_material_basis_in mutations in the CFH gene on chromosome 1q31.3. | ||
| Also Known As | "cuticular drusen" ; "drusen of bruch membrane" ; "early adult-onset grouped drusen" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
degeneration of macula and posterior pole |__retinal drusen_____ genetic disease | |__monogenic disease__| basal laminar drusen |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
monogenic disease retinal drusen |
||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
|
ICD10CM:H35.5 MESH:C563034 MIM:126700 ORDO:75376 |
|||