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 7 ID (Ontology) DOID:0110605 (Human Disease)
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.
Also Known As "CILD7" ; "primary ciliary dyskinesia 7 with or without situs inversus"
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 primary ciliary dyskinesia 7       2
 for disease ribbon | primary ciliary dyskinesia 7       2
 model of | primary ciliary dyskinesia 7       2
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  ciliopathy
   |__primary ciliary dyskinesia
       |__primary ciliary dyskinesia 7  2 rec.
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Synonyms
  • "CILD7" EXACT OMO:0003012
    "primary ciliary dyskinesia 7 with or without situs inversus" EXACT
Secondary IDs
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ICD10CM:Q34.8
MIM:611884