OBO ID: DOID:0110605
Term Name: primary ciliary dyskinesia 7 Search Ontology:
Synonyms:
  • CILD7
  • primary ciliary dyskinesia 7 with or without situs inversus
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
References:
Ontology: Human Disease   ( DOID:0110605 )
Relationships
is a type of:
OTHER primary ciliary dyskinesia 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DNAH11 Ciliary dyskinesia, primary, 7, with or without situs inversus 611884
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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