OBO ID: DOID:0110615
Term Name: primary ciliary dyskinesia 25 Search Ontology:
Synonyms:
  • CILD25
  • primary ciliary dyskinesia 25 with or without situs inversus
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, recurrent upper and lower airway disease, bronchiectasis, decreased fertility and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the DYX1C1 gene on chromosome 15q21. (2)
References:
Ontology: Human Disease   ( DOID:0110615 )
Relationships
is a type of:
OTHER primary ciliary dyskinesia 25 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DNAAF4 Ciliary dyskinesia, primary, 25 615482
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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