Fetal Prader-Willi syndrome risk   LP185770-7

LOINC Hierarchy


LOINC part codeLP185770-7
nameFetal Prader-Willi syndrome risk
typeCOMPONENT
statusACTIVE
children
LOINC Home
   {component}   LP432695-7
      Laboratory   LP29693-6
         Molecular pathology   LP7822-2
            Genetic screen   LP19405-7
               Deletions   LP7823-0
                  Fetal Prader-Willi syndrome risk   LP185770-7

Fetal Prader-Willi syndrome risk | Plasma cell-free+WBC DNA | Deletions   LP410593-0


Copyright © 2023 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2023, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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