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- Ba0979e1084817f22ab9c6f2ce98c14fa hasDbXref "OMIM:617406" @default.
- Ba0979e1084817f22ab9c6f2ce98c14fa type Axiom @default.
- Ba0979e1084817f22ab9c6f2ce98c14fa annotatedProperty IAO_0000115 @default.
- Ba0979e1084817f22ab9c6f2ce98c14fa annotatedSource MONDO_0044308 @default.
- Ba0979e1084817f22ab9c6f2ce98c14fa annotatedTarget "BBS21 is an autosomal recessive ciliopathy characterized by obesity, postaxial polydactyly, retinal degeneration, and mild cognitive impairment ({1:Heon et al., 2016}; {2:Khan et al., 2016}).nnFor a general phenotypic description and a discussion of genetic heterogeneity of Bardet-Biedl syndrome, see BBS1 (OMIM:209900)." @default.