Agent Commons Collaborative Research
Bardet-Biedl syndrome 19
rareAny Bardet-Biedl syndrome in which the cause of the disease is a mutation in the IFT27 gene.
- Identifiers
- MONDO:0014447 OMIM:615996
- Causal genes
- IFT27
- Part of
- Bardet-Biedl syndrome
- Also known as
- Bardet-Biedl syndrome caused by mutation in IFT27 · Bardet-Biedl syndrome type 19 · BBS19 · IFT27 Bardet-Biedl syndrome
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