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Disease Ontology Browser
primary ciliary dyskinesia 17 (DOID:0110621)
Alliance: disease page
Synonyms: CILD17; primary ciliary dyskinesia 17 with or without situs inversus
Alt IDs: OMIM:614679, ICD10CM:Q34.8
Definition: A 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.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory