| CLASS | MOLPATH.MUT | LP7824-8 |
| COMPONENT | Kallmann syndrome gene targeted mutation analysis | LP228778-9 |
| 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 | Both |
| LONG_COMMON_NAME | en-US | Kallmann syndrome gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal |
| LONG_COMMON_NAME | en-US | Kallmann syndrome gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal |
| SHORTNAME | en-US | KMS gene Mut Anl Bld/T |
| ConsumerName | en-US | Kallmann syndrome gene targeted mutation analysis, Blood or tissue specimen |
| SHORTNAME | es-AR | análisis de la mutación del gen del síndrome de Kallman:presencia o identidad:punto en el tiempo:sangre entera/tejido:Nominal:genética molecular |
| SHORTNAME | pt-BR | KMS gene Mut Anal Sg/T |
| LONG_COMMON_NAME | fr-FR | Syndrome de Kallmann gène mutation cible trouvée [Identification] Sang/Tissu ; Résultat nominal ; Biologie moléculaire |
| LONG_COMMON_NAME | nl-NL | Kallman-syndroom gen doelgerichte mutatie-analyse [identificator] in bloed of weefsel d.m.v. moleculair genetisch onderzoek |
| LONG_COMMON_NAME | es-MX | Análisis de mutaciones dirigidas al gen del síndrome de Kallmann: Sangre o tejido : Punto temporal: Presencia o identidad: Nominal: Genética molecular |
LOINC Version: 2.80
FHIR