OBO ID: DOID:0110612
Term Name: primary ciliary dyskinesia 10 Search Ontology:
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 primary ciliary dyskinesia 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DNAAF2 Ciliary dyskinesia, primary, 10 612518
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.