|
General Information
|
| Term |
polycystic kidney disease 1 |
ID (Ontology) |
DOID:0110858 (Human Disease) |
| Definition |
A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3. |
| Also Known As |
"APKD1" ; "PKD1" ; "Polycystic Kidney Disease, Adult, Type I" |
| 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 |
|---|
polycystic kidney disease 1 | 5 | for disease ribbon | polycystic kidney disease 1 | 5 | model of | polycystic kidney disease 1 | 5 |
|
Relationships