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Disease Ontology Browser
Bardet-Biedl syndrome 13 (DOID:0110135)
Alliance: disease page
Synonyms: BBS13
Alt IDs: OMIM:615990, ICD10CM:Q87.89
Definition: A Bardet-Biedl syndrome that has material basis in compound heterozygous mutation in the MKS1 gene on chromosome 17q22.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/04/2018
MGI 6.13
The Jackson Laboratory