obsolete_Bardet-Biedl syndrome 7 true 3.88.0 OMIM:615984 Replaced by Mondo term MONDO_0014435, with which this term was previously merged. Use: http://purl.obolibrary.org/obo/MONDO_0014435 BBS7 is an autosomal recessive disorder characterized by retinitis pigmentosa, postaxial polydactyly, intellectual disability, obesity, renal anomalies, and hypogenitalism (Harville et al., 2010). Zaghloul and Katsanis (2009) estimated the contribution of BBS7 gene mutations to the total BBS mutational load to be 1.50%. http://purl.obolibrary.org/obo/MONDO_0014435 Orphanet:118990 Hannah McLaren