Kartagener Syndrome

Preferred Label : Kartagener Syndrome;

NCIt definition : A rare autosomal recessive inherited syndrome characterized by situs inversus, bronchiectasis, and chronic sinusitis. There is a defect in the function of the cilia that line the respiratory tract.;

Details

Origin ID

C84797;

UMLS CUI

C0022521;

Automatic exact mappings (from CISMeF team)
- Immotile cilia syndrome [PASCAL descriptor]
Currated CISMeF NLP mapping
- Ciliary dyskinesia, primary, 1 [OMIM Phenotype]
- Kartagener syndrome [DO Concept]
- Kartagener syndrome [Disease (Nov.)]
- Kartagener syndrome [MeSH Descriptor]
- Kartagener syndrome (disorder) [SNOMED CT concept]
- Kartagener's syndrome [MedDRA LLT]
- Primary ciliary dyskinesia, Kartagener type [ICD-11 More detail]
- Primary ciliary dyskinesia, Kartagener type [ORDO Disease]
- kartagener syndrome [MeSH concept]
- kartagener syndrome [SNOMED Notion]
DO Cross reference
- Kartagener syndrome [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Kartagener syndrome [DO Concept]
- Kartagener syndrome [Disease (Nov.)]
- Kartagener syndrome [MeSH Descriptor]
- Kartagener syndrome (disorder) [SNOMED CT concept]
- Kartagener's syndrome [MedDRA LLT]
- Primary ciliary dyskinesia, Kartagener type [ORDO Disease]
- kartagener syndrome [SNOMED Notion]
- kartagener syndrome [MeSH concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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