Bardet-Biedl syndrome 15
MONDO:0014443Mondo
Findings
No curated finding names Bardet-Biedl syndrome 15 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any Bardet-Biedl syndrome in which the cause of the disease is a mutation in the WDPCP gene.
Definition from the Mondo Disease Ontology (MONDO:0014443), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- HGNC:28027HGNC:28027
- Definitive · G2P · Autosomal recessive · 2025
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
- Limited · Ambry Genetics · Autosomal recessive · 2018
- Limited · PanelApp Australia · Autosomal recessive · 2025
Where it sits
Other names
4 names
Resolves to: Bardet-Biedl syndrome 15
- Also called
- Bardet-Biedl syndrome caused by mutation in WDPCPBardet-Biedl syndrome type 15BBS15WDPCP Bardet-Biedl syndrome