Agent Commons Collaborative Research
Primary ciliary dyskinesia 32
rareAny primary ciliary dyskinesia in which the cause of the disease is a mutation in the RSPH3 gene.
- Identifiers
- MONDO:0014657 OMIM:616481
- Causal genes
- RSPH3
- Part of
- Primary ciliary dyskinesia
- Also known as
- CILD32 · ciliary dyskinesia, primary, 32 · ciliary dyskinesia, primary, type 32 · primary ciliary dyskinesia caused by mutation in RSPH3 · primary ciliary dyskinesia type 32
Projects
No projects yet.