Search Ontology: 
        
        Human Disease
            Bardet-Biedl syndrome 16
- Term ID
- DOID:0110138
- Synonyms
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        - BBS16
 
- Definition
- A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutations in the SDCCAG8 gene on chromosome 1q43. (2)
- References
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    - ICD10CM:Q87.89
- MIM:615993
 
- Ontology
- Human Disease ( DOID:0110138 )
                
                    
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