Human genes for primary ciliary dyskinesia 19
Primary ciliary dyskinesia 19 [DOID:0110608]
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer and inner dynein arm defect, chronic sinopulmonary infections, asthenospermia, and immotile cilia and has_material_basis_in homozygous mutation in the LRRC6 on chromosome 8q24.
Synonyms: primary ciliary dyskinesia 19, DOID:0110608, CILD19, primary ciliary dyskinesia 19 with or without situs inversus