Search Ontology:
Human Disease

primary ciliary dyskinesia 10

Term ID
DOID:0110612
Synonyms
  • CILD10
  • primary ciliary dyskinesia 10 with or without situs inversus
Definition
A primary ciliary dyskinesia that is characterized by outer and inner dynein arm absence, chronic otitis media, sinusitis, recurrent pneumonia and variable occurrence of situs inversus and has_material_basis_in homozygous mutation in the KTU gene on chromosome 14q21. https://www.ncbi.nlm.nih.gov/pubmed/19052621
References
Ontology
Human Disease   ( DOID:0110612 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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