Variants
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Primary ciliary dyskinesia 30

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Description

Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the CCDC151 gene.

MONDO

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

77

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Genes

External Links

  • OMIM

    616037

  • Orphanet
  • HPO
  • Medgen

    C4015016

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