| CLASS | HL7.GENETICS | LP70593-6 |
| COMPONENT | Genetic disease sequence variation interpretation | LP69972-5 |
| 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 | ACMG_Clinical significance of genetic variation | LL4034-6 |
| parent | Genetic disease sequence variation interpretation | Blood or Tissue | HL7 genetics | LP410557-5 |
| CLASSTYPE | Laboratory class | |
| ORDER_OBS | Observation | |
| UNITSREQUIRED | N |
| LONG_COMMON_NAME | en-US | Genetic variation clinical significance [Imp] |
| LONG_COMMON_NAME | en-US | Genetic variation clinical significance [Imp] |
| SHORTNAME | en-US | Gene dis seq var interp-Imp |
| ConsumerName | en-US | Genetic disease sequence variation interpretation, Blood or tissue specimen |
| SHORTNAME | pt-BR | Gene dis seq var interp Sg/T-Imp |
| LONG_COMMON_NAME | fr-FR | Maladie génétique interprétation globale de la variation de séquence [Interprétation] Sang/Tissu ; Résultat nominal ; Biologie moléculaire |
| LONG_COMMON_NAME | nl-NL | Genetische ziekte sequentievariatie interpretatie [interpretatie] in bloed of weefsel d.m.v. moleculair genetisch onderzoek |
| LONG_COMMON_NAME | es-MX | Interpretación de la variación de la secuencia de la enfermedad genética: Sangre o tejido : Punto temporal: Impresión / interpretación del estudio: Nominal: Genética molecular |
LOINC Version: 2.77
FHIR