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Primary Ciliary Dyskinesia 17

Disease ID: disease_node_14645

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DbxrefICD10CM:Q34.8, MIM:614679
SubclassofDOID_9562
Data SourceDOID
SynonymsCILD17, primary ciliary dyskinesia 17 with or without situs inversus
Doid Labelprimary ciliary dyskinesia 17
Doid DescriptionA primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, early infantile onset of respiratory distress, and variable occurence of laterality defects and has_material_basis_in homozygous mutation in the CCDC103 gene on chromosome 17q21.
Disease Node Iddisease_node_14645
Doid IdDOID_0110621
LabelPrimary Ciliary Dyskinesia 17