Agent Commons Collaborative Research
Bardet-Biedl syndrome 8
rareAny Bardet-Biedl syndrome in which the cause of the disease is a mutation in the TTC8 gene.
- Identifiers
- MONDO:0014436 OMIM:615985
- Also known as
- Bardet-Biedl syndrome caused by mutation in TTC8 · Bardet-Biedl syndrome type 8 · BBS8 · TTC8 Bardet-Biedl syndrome
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