Bardet-Biedl syndrome 15

Bardet-Biedl syndrome that has material basis in homozygous mutation in the WDPCP gene on chromosome 2p15
rdfs:label "Bardet-Biedl syndrome 15"@en
skos:altLabel "BARDET-BIEDL SYNDROME 15"@en
"BARDET-BIEDL SYNDROME 15; BBS15"@en
"BBS15"@en
"Bardet-Biedl syndrome type 15"@en
schema:description
"Bardet-Biedl syndrome that has material basis in homozygous mutation in the WDPCP gene on chromosome 2p15"@en
schema:dateModified "2025-07-21T15:38:35+00:00"^^xsd:dateTime
schema:version 2382433950
wikibase:identifiers 6
wikibase:sitelinks 0
wikibase:statements 14
p:P11430 wd:statement/Q27674841-4e3f20bc-4d60-89ec-ab30-441cbcf6ad6a
p:P1995 wd:statement/Q27674841-E5CE5DE1-1DD7-4542-9280-B3FA5752EF47
p:P2293 wd:statement/Q27674841-E676E326-114F-4832-814C-C0238846790C
p:P279 wd:statement/Q27674841-09BBE328-2A30-4C5D-ACE4-CBDE0B593221
p:P2888 wd:statement/Q27674841-09F5724D-7CB5-464A-BC13-37B9221A91C3
wd:statement/Q27674841-0FBE54EF-F10D-4B8F-89F8-474EAD8106FF
p:P2892 wd:statement/Q27674841-3A1875E4-AD65-42AD-8401-5C08B8DEB67B
p:P31 wd:statement/Q27674841-CE7F1908-9A21-4794-AB38-AF01066660EF
wd:statement/Q27674841-DCD1A825-7B62-4F93-AFCF-E34606CEEF6F
p:P4229 wd:statement/Q27674841-BBA1E3FD-347E-48E1-BC83-8D711F452EDA
p:P492 wd:statement/Q27674841-F8A78F96-D66E-41F9-AFF9-62ECCB8B21B7
p:P5008 wd:statement/Q27674841-64C54C23-9915-48EF-A7AB-EA85F27C0BA9
p:P5270 wd:statement/Q27674841-65F13D67-3E48-4FF6-89ED-2010EE56465A
p:P699 wd:statement/Q27674841-CFA70DC7-3D38-4053-9BBC-FCA9452F3D17
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0014443>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0110137>
wdt:P11430 "DI-02938"
wdt:P1995 medical genetics
wdt:P2293 WDPCP
wdt:P279 Bardet-Biedl syndrome
wdt:P2888 <http://identifiers.org/doid/DOID:0110137>
<http://purl.obolibrary.org/obo/DOID_0110137>
wdt:P2892 "C3150127"
wdt:P31 type of disease
rare disease
wdt:P4229 "Q87.89"
wdt:P492 "615992"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0014443"
wdt:P699 "DOID:0110137"
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