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Disease Ontology Browser
primary ciliary dyskinesia 15 (DOID:0110623)
Alliance: disease page
Synonyms: CILD15; primary ciliary dyskinesia 15 with or without situs inversus
Alt IDs: OMIM:613808, ICD10CM:Q34.8
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner dynein arm defect, axonemal disorganization, recurrent respiratory infections and has_material_basis_in homozygous or compound heterozygous mutation in the CCDC40 gene on chromosome 17q25.


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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