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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Bardet-Biedl syndrome +     
Bardet-Biedl syndrome 1 +   
Bardet-Biedl syndrome 10 +   
Bardet-Biedl syndrome 11  
Bardet-Biedl syndrome 12  
Bardet-Biedl syndrome 13  
Bardet-Biedl syndrome 14  
Bardet-Biedl syndrome 15  
Bardet-Biedl syndrome 16  
Bardet-Biedl syndrome 17  
Bardet-Biedl syndrome 18  
Bardet-Biedl syndrome 19  
Bardet-Biedl syndrome 2 +   
Bardet-Biedl syndrome 20  
Bardet-Biedl syndrome 21  
Bardet-Biedl syndrome 22  
A Bardet-Biedl syndrome that is retinitis pigmentosa, obesity, polydactyly, hypogonadism, and intellectual disability has_material_basis_in compound heterozygous or homozygous mutation in the IFT74 gene on chromosome 9p21. (DO)
Bardet-Biedl syndrome 3  
Bardet-Biedl syndrome 4 +   
Bardet-Biedl syndrome 5  
Bardet-Biedl syndrome 6 +   
Bardet-Biedl syndrome 7 +   
Bardet-Biedl syndrome 8  
Bardet-Biedl syndrome 9  

Synonyms
Exact Synonyms: BBS22
Related Synonyms: BBS20 (formerly) ;   Bardet-Biedl syndrome 20 (formerly)
Primary IDs: OMIM:617119
Alternate IDs: DOID:9004483
Definition Sources: https://pubmed.ncbi.nlm.nih.gov/27486776/ "DO" "DO"

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