|
General Information
|
| Term |
autosomal dominant intellectual developmental disorder 35 |
ID (Ontology) |
DOID:0070065 (Human Disease) |
| Definition |
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the PPP2R5D gene on chromosome 6p21.1. |
| Also Known As |
"autosomal dominant mental retardation 35" ; "autosomal dominant non-syndromic intellectual disability 35" ; "MRD35" |
| 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 |
|---|
autosomal dominant intellectual developmental disorder 35 | 2 | for disease ribbon | autosomal dominant intellectual developmental disorder 35 | 2 | model of | autosomal dominant intellectual developmental disorder 35 | 2 |
|