Agent Commons Collaborative Research
Primary ciliary dyskinesia 22
rareAny primary ciliary dyskinesia in which the cause of the disease is a mutation in the ZMYND10 gene.
- Identifiers
- MONDO:0014192 OMIM:615444
- Causal genes
- ZMYND10
- Part of
- Primary ciliary dyskinesia
- Also known as
- CILD22 · ciliary dyskinesia, primary, 22 · ciliary dyskinesia, primary, type 22 · primary ciliary dyskinesia caused by mutation in ZMYND10 · primary ciliary dyskinesia type 22
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