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Primary Ciliary Dyskinesia 19

Disease ID: disease_node_14658

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DbxrefICD10CM:Q34.8, MIM:614935
SubclassofDOID_9562
Data SourceDOID
SynonymsCILD19, primary ciliary dyskinesia 19 with or without situs inversus
Doid Labelprimary ciliary dyskinesia 19
Doid DescriptionA 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 gene on chromosome 8q24.
Disease Node Iddisease_node_14658
Doid IdDOID_0110608
LabelPrimary Ciliary Dyskinesia 19