OBO ID: DOID:0110620
Term Name: primary ciliary dyskinesia 35 Search Ontology:
Synonyms:
  • CILD35
  • primary ciliary dyskinesia 35 with or without situs inversus
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with absent outer dynein arms, immotile cilia, variable occurence of laterality defects and recurrent upper and lower respiratory infections and has_material_basis_in homozygous mutation in the TTC25 gene on chromosome 17q21. https://www.ncbi.nlm.nih.gov/pubmed/27486780
References:
Ontology: Human Disease   ( DOID:0110620 )
Relationships
is a type of:
OTHER primary ciliary dyskinesia 35 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TTC25 Ciliary dyskinesia, primary, 35 617092
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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