Bardet-Biedl syndrome 10

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Summary

Literature (0)

DOID:0110132 - Bardet-Biedl syndrome 10

Disease Ontology Definition:A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the BBS10 gene on chromosome 12q21.

Synonyms: BBS10

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: bbs10

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014438 - Bardet-Biedl syndrome 10

MONDO:0014438 - Bardet-Biedl syndrome 10

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): Bardet-Biedl syndrome (is_a)