Genetic variant clinical significance - CISMeF

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CISMeF

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Genetic variant clinical significanceLOINC component

Preferred Label : Genetic variant clinical significance;

LOINC status : ACTIVE;

UMLS MTHU# : MTHU025338;

Details

Origin ID

LP62054-9;

UMLS CUI

C1953337;

LOINC code(s)
- Genetic variant clinical significance:Imp:Pt:Bld/Tiss:Nom:Molgen [LOINC code]
Semantic type(s)
- Finding [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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30/05/2025

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