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Metadata
ID	DOID:0110627
Name	primary ciliary dyskinesia 26
Definition	A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, neonatal respiratory distress, recurrent upper and lower airway disease, bronchiectasis, and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the C21ORF59 gene on chromosome 21q22. https://www.ncbi.nlm.nih.gov/pubmed/24094744, https://www.ncbi.nlm.nih.gov/pubmed/26998415
Xrefs	ICD10CM:Q34.8 OMIM:615500
Synonyms	CILD26 [EXACT] primary ciliary dyskinesia 26 with or without situs inversus [EXACT]
Parent Relationships	is_a primary ciliary dyskinesia