Bardet-Biedl syndrome 8

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Summary

Literature (0)

DOID:0110130 - Bardet-Biedl syndrome 8

Disease Ontology Definition:A Bardet-Biedl syndrome that has_material_basis_in homozygous mutation in the TTC8 gene on chromosome 14q31.

Synonyms: BBS8

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

: ttc8

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014436 - Bardet-Biedl syndrome 8

MONDO:0014436 - Bardet-Biedl syndrome 8

MIM:

MIM:615985 - BARDET-BIEDL SYNDROME 8; BBS8

MIM:615985 - BARDET-BIEDL SYNDROME 8; BBS8

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)