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DO Term : primary ciliary dyskinesia 7 [DOID:0110605] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • primary ciliary dyskinesia 7 with or without situs inversus,
  • CILD7,
  • 611884,
  • OMIM:611884,
  • ICD10CM:Q34.8
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Ontology Term --> Direct children

Ontology Term --> Direct parents