Visualize Submit Comment
Metadata
ID DOID:0110605
Name primary ciliary dyskinesia 7
Definition A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with chronic respiratory infections, chronic sinusitis, recurrent bronchitis, and pneumonia beginning in infancy or early childhood and has_material_basis_in mutation in the DNAH11 gene on chromosome 7p21.
https://www.ncbi.nlm.nih.gov/pubmed/18022865
Xrefs

ICD10CM:Q34.8

OMIM:611884

Synonyms

CILD7 [EXACT]

primary ciliary dyskinesia 7 with or without situs inversus [EXACT]

Parent Relationships

is_a primary ciliary dyskinesia

Add an item to the term tracker