| CLASS | MOLPATH | LP7822-2 |
| COMPONENT | KIR3DP1 gene deletion variant | LP117775-9 |
| PROPERTY | PrThr | LP217195-9 |
| TIME_ASPCT | Pt | LP6960-1 |
| SYSTEM | Bld/Tiss | LP7061-7 |
| SCALE_TYP | Ord | LP7751-3 |
| METHOD_TYP | Molgen | LP6404-0 |
| AnswerList | Present|Absent | LL1937-3 |
| parent | KIR3DP1 gene deletion variant | Blood or Tissue | Molecular pathology | LP401713-5 |
| CLASSTYPE | Laboratory class | |
| ORDER_OBS | Observation | |
| UNITSREQUIRED | N |
| LONG_COMMON_NAME | en-US | KIR3DP1 gene deletion variant [Presence] in Blood or Tissue by Molecular genetics method |
| LONG_COMMON_NAME | en-US | KIR3DP1 gene deletion variant [Presence] in Blood or Tissue by Molecular genetics method |
| SHORTNAME | en-US | KIR3DP1 del variant Bld/T Ql |
| ConsumerName | en-US | KIR3DP1 gene Deletion variant, Blood or tissue specimen |
| LONG_COMMON_NAME | fr-FR | KIR3DP1 gène délétion variant [Présence/Seuil] Sang/Tissu ; Qualitatif ; Biologie moléculaire |
| LONG_COMMON_NAME | nl-NL | KIR-allel 3DP1 DEL [aanwezigheid] in bloed of weefsel d.m.v. moleculair genetisch onderzoek |
| LONG_COMMON_NAME | es-MX | Variante de deleción del gen KIR3DP1: Sangre o tejido : Punto temporal: Presencia o umbral: Ordinal: Genética molecular |
LOINC Version: 2.77
FHIR