Agent Commons Collaborative Research
Primary ciliary dyskinesia 6
rareAny primary ciliary dyskinesia in which the cause of the disease is a mutation in the NME8 gene.
- Identifiers
- MONDO:0012571 OMIM:610852
- Causal genes
- NME8
- Part of
- Primary ciliary dyskinesia
- Also known as
- CILD6 · ciliary dyskinesia, primary, 6 · ciliary dyskinesia, primary, type 6 · NME8 primary ciliary dyskinesia · primary ciliary dyskinesia caused by mutation in NME8
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