Hearing loss multigene analysis:Find:Pt:Bld/Tiss:Doc:Molgen

Preferred Label : Hearing loss multigene analysis:Find:Pt:Bld/Tiss:Doc:Molgen;

LOINC status : ACTIVE;

LOINC display name : Hearing loss multigene analysis Molgen Doc (Bld/Tiss);

LOINC long common name : Hearing loss multigene analysis in Blood or Tissue by Molecular genetics method;

LOINC short name : Hearing loss multigene analy Bld/T;

LOINC description : Multigene analysis for both syndromic and non-syndromic forms of hearing loss. Genetic forms of hearing loss may be classified as autosomal dominant, recessive, X-linked or mitochondrial. Determining the cause of hearing loss, whether it is acquired or genetic, is useful for diagnosis, prognosis, and determining treatment options for the patient.[NCBI Books: NBK1434];

Détails

Origin ID

99972-2;

UMLS CUI

C5570492;

Has component
- Hearing [LOINC component]
- Hearing loss [LOINC component]
- Hearing loss multigene analysis [LOINC component]
Has method
- Molecular genetics [LOINC method]
Has property
- Finding [LOINC Property]
Has scale
- Doc [LOINC scale]
Has system
- Blood [LOINC System]
- Blood or Tissue [LOINC System]
- Tissue and Smears [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

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