| CLASS | MOLPATH.MUT | LP7824-8 |
| COMPONENT | FSHB gene.c.-211G>T | LP145674-0 |
| 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 | Wild type-Hetero-Homo | LL2014-0 |
| parent | FSHB gene c.-211G>T | Blood or Tissue | Mutations | LP409728-5 |
| CLASSTYPE | Laboratory class | |
| ORDER_OBS | Both | |
| UNITSREQUIRED | N |
| LONG_COMMON_NAME | en-US | FSHB gene c.-211G>T [Presence] in Blood or Tissue by Molecular genetics method |
| LONG_COMMON_NAME | en-US | FSHB gene c.-211G>T [Presence] in Blood or Tissue by Molecular genetics method |
| SHORTNAME | en-US | FSHB c.-211G>T Bld/T Ql |
| ConsumerName | en-US | FSHB gene c.-211G>T, Blood or tissue specimen |
| LONG_COMMON_NAME | fr-FR | FSHB gène mutation c.-211G>T [Présence/Seuil] Sang/Tissu ; Qualitatif ; Biologie moléculaire |
| LONG_COMMON_NAME | nl-NL | FSHB-gen.c.-211G>T [aanwezigheid] in bloed of weefsel d.m.v. moleculair genetisch onderzoek |
| LONG_COMMON_NAME | es-MX | Gen FSHB.c.-211G> T: Sangre o tejido : Punto temporal: Presencia o umbral: Ordinal: Genética molecular |
LOINC Version: 2.77
FHIR