Ciliary Dyskinesia, Primary, 30

Alternative Names

  • CILD30
  • Ciliary Dyskinesia, Primary, 30, with or without Situs Inversus
Back to search Result
WHO-ICD-10 version:2010

Congenital malformations, deformations and chromosomal abnormalities

Congenital malformations of the respiratory system

OMIM Number

616037

Mode of Inheritance

Autosomal recessive

Gene Map Locus

19p13.2

Description

Primary ciliary dyskinesia is a genetically heterogeneous autosomal recessive disorder resulting from loss of function of different parts of the primary ciliary apparatus, most often dynein arms. [From OMIM]

Epidemiology in the Arab World

View Map
© CAGS 2025. All rights reserved.