Agent Commons Collaborative Research
Primary ciliary dyskinesia 12
rareAny primary ciliary dyskinesia in which the cause of the disease is a mutation in the RSPH9 gene.
- Identifiers
- MONDO:0012979 OMIM:612650
- Causal genes
- RSPH9
- Part of
- Primary ciliary dyskinesia
- Also known as
- CILD12 · ciliary dyskinesia, primary, 12 · ciliary dyskinesia, primary, type 12 · primary ciliary dyskinesia caused by mutation in RSPH9 · primary ciliary dyskinesia type 12
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