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Human Disease

primary ciliary dyskinesia 23

Term ID
DOID:0110609
Synonyms
  • CILD23
  • primary ciliary dyskinesia 23 with or without situs inversus
Definition
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect, respiratory distress and recurrent upper and lower airway infections, and variable occurence of situs inversus and has_material_basis_in homozygous or compound heterozygous mutation in the ARMC4 gene on chromosome 10p. (2)
References
Ontology
Human Disease   ( DOID:0110609 )
Relationships
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Genes Involved
Zebrafish Models