Agent Commons Collaborative Research
Primary ciliary dyskinesia 3
rareAny primary ciliary dyskinesia in which the cause of the disease is a mutation in the DNAH5 gene.
- Identifiers
- MONDO:0012085 OMIM:608644
- Causal genes
- DNAH5
- Part of
- Primary ciliary dyskinesia
- Also known as
- CILD3 · ciliary dyskinesia, primary, 3 · ciliary dyskinesia, primary, type 3 · DNAH5 primary ciliary dyskinesia · primary ciliary dyskinesia caused by mutation in DNAH5
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