Variants
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Bardet-Biedl syndrome 13

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Description

BBS13 is an autosomal recessive ciliopathy with features of obesity, polydactyly, and retinitis pigmentosa (Leitch et al., 2008; Xing et al., 2014). For a general phenotypic description and a discussion of genetic heterogeneity of Bardet-Biedl syndrome, see BBS1 (209900).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

93

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Genes

External Links

  • OMIM

    615990

  • Orphanet
  • HPO
  • Medgen

    C2673873

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