| CLASS | MOLPATH.MUT | LP7824-8 |
| COMPONENT | CATCH22 syndrome gene mutations tested for | LP227915-8 |
| PROPERTY | Prid | LP6850-4 |
| TIME_ASPCT | Pt | LP6960-1 |
| SYSTEM | Bld/Tiss | LP7061-7 |
| SCALE_TYP | Nom | LP7750-5 |
| METHOD_TYP | Molgen | LP6404-0 |
| parent | Lab terms not yet categorized | LP248770-2 |
| CLASSTYPE | Laboratory class | |
| ORDER_OBS | Observation | |
| UNITSREQUIRED | N |
| LONG_COMMON_NAME | en-US | CATCH22 syndrome gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal |
| LONG_COMMON_NAME | en-US | CATCH22 syndrome gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal |
| SHORTNAME | en-US | CATCH22 gene Mut Tested Bld/T |
| ConsumerName | en-US | CATCH22 syndrome gene variants tested for, Blood or tissue specimen |
| SHORTNAME | es-AR | gen del síndrome CATCH22 :presencia o identidad:punto en el tiempo:tejido, no especificado:Nominal:genética molecular |
| SHORTNAME | pt-BR | CATCH22 gene Mut Tested Sg/T |
| LONG_COMMON_NAME | fr-FR | CATCH22 gène mutations recherchées [Identification] Sang/Tissu ; Résultat nominal ; Biologie moléculaire |
| LONG_COMMON_NAME | nl-NL | CATCH22-syndroomgen geteste mutaties [identificator] in bloed of weefsel d.m.v. moleculair genetisch onderzoek |
| LONG_COMMON_NAME | es-MX | Mutaciones del gen del síndrome CATCH22 analizadas para: Sangre o tejido : Punto temporal: Presencia o identidad: Nominal: Genética molecular |
LOINC Version: 2.80
FHIR