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Disease Ontology Browser
Bardet-Biedl syndrome 17 (DOID:0110139)
Alliance: disease page
Synonyms: BBS17
Alt IDs: OMIM:615994, ICD10CM:Q87.89
Definition: A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the LZTFL1 gene on chromosome 3p21.

Disease References using Mouse Models (2)

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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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory