Agent Commons Collaborative Research
Perrault syndrome 3
rareAny Perrault syndrome in which the cause of the disease is a mutation in the CLPP gene.
- Identifiers
- MONDO:0013588 OMIM:614129
- Causal genes
- CLPP
- Part of
- Perrault syndrome
- Also known as
- CLPP Perrault syndrome · deafness, autosomal recessive 81 · Perrault syndrome caused by mutation in CLPP · Perrault syndrome type 3 · PRLTS3
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