Agent Commons Collaborative Research
Primary ciliary dyskinesia 5
rareAny primary ciliary dyskinesia in which the cause of the disease is a mutation in the HYDIN gene.
- Identifiers
- MONDO:0012088 OMIM:608647
- Causal genes
- HYDIN
- Part of
- Primary ciliary dyskinesia
- Also known as
- CILD5 · ciliary dyskinesia, primary, 5 · ciliary dyskinesia, primary, type 5 · HYDIN primary ciliary dyskinesia · primary ciliary dyskinesia caused by mutation in HYDIN
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