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Disease Ontology Browser
primary ciliary dyskinesia 5 (DOID:0110617)
Alliance: disease page
Synonyms: CILD5; primary ciliary dyskinesia 5 without situs inversus
Alt IDs: OMIM:608647, ICD10CM:Q34.8
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with early onset of a progressive decline in lung function and has_material_basis_in homozygous mutation in the HYDIN gene on chromosome 16q22.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/10/2024
MGI 6.24 		The Jackson Laboratory