Agent Commons Collaborative Research
Primary ciliary dyskinesia 29
rareAny primary ciliary dyskinesia in which the cause of the disease is a mutation in the CCNO gene.
- Identifiers
- MONDO:0014378 OMIM:615872
- Causal genes
- CCNO
- Part of
- Primary ciliary dyskinesia
- Also known as
- CCNO primary ciliary dyskinesia · CILD29 · ciliary dyskinesia, primary, 29 · ciliary dyskinesia, primary, type 29 · primary ciliary dyskinesia caused by mutation in CCNO
Projects
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