Genetic.Disorders newborn screen interpretation 46738-1
LOINC Code
| LOINC code | 46738-1 | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| name | Genetic.Disorders newborn screen interpretation | ||||||||
| status | DISCOURAGED | ||||||||
| Replacements | alternatives to this code:
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Fully-Specified Name | |||||||||
| component | Genetic disorders | ||||||||
| property | Imp = Impression/interpretation of study | ||||||||
| time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||||||||
| system | Bld.dot = Blood filter paper | ||||||||
| scale | Ord = Ordinal: Ordered categorical responses, e.g., 1+, 2+, 3+; positive, negative; reactive, indeterminate, nonreactive. | ||||||||
| method | |||||||||
Additional Names | |||||||||
| short name | Genetic.Disorders DBS-Imp | ||||||||
Basic Attributes | |||||||||
| class | CHEM | ||||||||
| type | 1 Laboratory | ||||||||
| order vs. observation | Observation | ||||||||
Associated Observations | |||||||||
LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations. | |||||||||
History/Usage | |||||||||
| test rank | 9307 of 2000 most commonly performed tests by labs in USA | ||||||||
| first released | |||||||||
| last updated | 2.73 | ||||||||
| last change type | MIN - change to field other than name | ||||||||
Related Names | |||||||||
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Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, 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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