genetische variant klinische significantie - CISMeF

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Genetische variant klinische significantieComposé LOINC

Voorkeurslabel : genetische variant klinische significantie;

UMLS MTHU# : MTHU025338;

Details

Oorsprong id

LP62054-9;

UMLS CUI

C1953337;

LOINC code(s)
- genetische variant klinische significantie:interpretatie:moment:bloed of weefsel:nominaal:moleculair genetisch onderzoek [LOINC code]

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20/07/2025

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