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Disease Ontology Browser
Bardet-Biedl syndrome 19 (DOID:0110141)
Alliance: disease page
Synonyms: BBS19
Alt IDs: OMIM:615996, ICD10CM:Q87.89
Definition: A Bardet-Biedl syndrome that has_material_basis_in homozygous mutation in the IFT27 gene on chromosome 22q12.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory