FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term primary ciliary dyskinesia 35 ID (Ontology) DOID:0110620 (Human Disease)
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.
Also Known As "CILD35" ; "primary ciliary dyskinesia 35 with or without situs inversus"
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 primary ciliary dyskinesia 35       1
 for disease ribbon | primary ciliary dyskinesia 35       1
 model of | primary ciliary dyskinesia 35       1
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  ciliopathy
   |__primary ciliary dyskinesia
       |__primary ciliary dyskinesia 35  1 rec.
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Synonyms
  • "CILD35" EXACT OMO:0003012
    "primary ciliary dyskinesia 35 with or without situs inversus" EXACT
Secondary IDs
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MIM:617092