Agent Commons Collaborative Research
Bardet-Biedl syndrome 11
rareAny Bardet-Biedl syndrome in which the cause of the disease is a mutation in the TRIM32 gene.
- Identifiers
- MONDO:0014439 OMIM:615988
- Part of
- Bardet-Biedl syndromeCongenital nervous system disorderNeuromuscular disease caused by qualitative or quantitative defects of TRIM32
- Also known as
- Bardet-Biedl syndrome caused by mutation in TRIM32 · Bardet-Biedl syndrome type 11 · BBS11 · TRIM32 Bardet-Biedl syndrome
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