| General Information | |||
|---|---|---|---|
| Term | primary ciliary dyskinesia 6 | ID (Ontology) | DOID:0110606 (Human Disease) |
| Definition | A primary ciliary dyskinesia that is characterized by partial outer dynein arm defect and has_material_basis_in mutation in the TXNDC3 gene on the chromosome 7p14.1. | ||
| Also Known As | "CILD6" | ||
| 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
|
|||
|
||||||
ciliopathy |__primary ciliary dyskinesia |__primary ciliary dyskinesia 6 2 rec. |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | primary ciliary dyskinesia | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
ICD10CM:Q34.8 MIM:610852 |
|||