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GTR Home > Conditions/Phenotypes > Bardet-Biedl syndrome 9

Bardet-Biedl syndrome 9

Summary

BBS9 is an autosomal recessive disorder characterized by obesity, polydactyly, renal anomalies, retinopathy, and mental retardation (Abu-Safieh et al., 2012). For a general phenotypic description and a discussion of genetic heterogeneity of Bardet-Biedl syndrome, see BBS1 (209900). [from OMIM]

Available tests

59 tests are in the database for this condition.

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Clinical tests (59 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: B1, C18, D1, PTHB1, BBS9
    Summary: Bardet-Biedl syndrome 9

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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