(Q28024727)

English

primary ciliary dyskinesia 21

primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with a missing Nexin link, infantile onset of chronic sinopulmonary infections, and has material basis in homozygous mutation in the DRC1 gene on chromosome 2p23

  • CILD21
  • primary ciliary dyskinesia 21 without situs inversus
  • Ciliary Dyskinesia, Primary, 21, Without Situs Inversus
  • CILIARY DYSKINESIA, PRIMARY, 21; CILD21
  • CILIARY DYSKINESIA, PRIMARY, 21
  • Ciliary Dyskinesia, Primary, type 21
  • primary ciliary dyskinesia type 21

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