Primary Ciliary Dyskinesia 10
Disease ID: disease_node_14654
Connections displayed (default: 10).
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| Dbxref | ICD10CM:Q34.8, MIM:612518 |
|---|---|
| Subclassof | DOID_9562 |
| Data Source | DOID |
| Synonyms | CILD10, primary ciliary dyskinesia 10 with or without situs inversus |
| Doid Label | primary ciliary dyskinesia 10 |
| Doid Description | A primary ciliary dyskinesia that is characterized by outer and inner dynein arm absence, chronic otitis media, sinusitis, recurrent pneumonia and variable occurrence of situs inversus and has_material_basis_in homozygous mutation in the KTU gene on chromosome 14q21. |
| Disease Node Id | disease_node_14654 |
| Doid Id | DOID_0110612 |
| Label | Primary Ciliary Dyskinesia 10 |
- Outgoing r'ship
SUBCLASS_OFto/from Ciliary Motility Disorders(ID:disease_node_2113) (Disease)