Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/615992 http://purl.bioontology.org/ontology/OMIM/615992
Preferred Name	BARDET-BIEDL SYNDROME 15
Synonyms	BBS15
Type	http://www.w3.org/2002/07/owl#Class

altLabel	BBS15
prefLabel	BARDET-BIEDL SYNDROME 15
Gene Symbol	BBS15 WDPCP CHDTHP C2orf86
Scope Statement	Based on report of 2 Pakistani sibs (last curated May 2024) [MISCELLANEOUS] Caused by mutation in the WD repeat-containing planar cell polarity effector gene (WDPCP, 613580.0001) [MOLECULAR BASIS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU038541 http://purl.bioontology.org/ontology/OMIM/MTHU008446 http://purl.bioontology.org/ontology/OMIM/MTHU000132 http://purl.bioontology.org/ontology/OMIM/MTHU001611 http://purl.bioontology.org/ontology/OMIM/MTHU002571 http://purl.bioontology.org/ontology/OMIM/MTHU000064 http://purl.bioontology.org/ontology/OMIM/MTHU000250 http://purl.bioontology.org/ontology/OMIM/MTHU078366 http://purl.bioontology.org/ontology/OMIM/MTHU025628 See more See less
tui	T047
Gene Locus	2p15
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	615992
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000016
cui	C3150127
OMIM Entry Type	3
OMIM MimType Value	pound

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