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LOINC Code 47997-2 : Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method

Properties

CLASS MOLPATH.MISC LP121011-3
COMPONENT Genetic variant clinical significance LP62054-9
PROPERTY Imp LP6819-9
TIME_ASPCT Pt LP6960-1
SYSTEM Bld/Tiss LP7061-7
SCALE_TYP Nom LP7750-5
METHOD_TYP Molgen LP6404-0
AnswerList MG_1_Genetic variant LL377-3
parent Lab terms not yet categorized LP248770-2
CLASSTYPE Laboratory class
ORDER_OBS Observation
UNITSREQUIRED N
STATUS ACTIVE

Displays

LONG_COMMON_NAME en-US Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method
LONG_COMMON_NAME en-US Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method
SHORTNAME en-US Genetic variant clin sig Bld/T-Imp
ConsumerName en-US Genetic variant clinical significance, Blood or tissue specimen
SHORTNAME pt-BR Genetic variant clin sig Sg/T-Imp
LONG_COMMON_NAME nl-NL Genetische variant klinische significantie [interpretatie] in bloed of weefsel d.m.v. moleculair genetisch onderzoek
LONG_COMMON_NAME es-MX Importancia clínica de la variante genética: Sangre o tejido : Punto temporal: Impresión / interpretación del estudio: Nominal: Genética molecular

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