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Primary ciliary dyskinesia 19

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Description

Primary ciliary dyskinesia-19 is an autosomal recessive ciliopathy characterized by chronic sinopulmonary infections, asthenospermia, and immotile cilia. Respiratory epithelial cells and sperm flagella of affected individuals lack both the inner and outer dynein arms. About 50% of patients have situs inversus (summary by Kott et al., 2012). For a phenotypic description and a discussion of genetic heterogeneity of primary ciliary dyskinesia, see 244400.

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

85

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Genes

External Links

  • OMIM

    614935

  • Orphanet
  • HPO
  • Medgen

    C3543826

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