Lifetime risk for developing genetic disease assessed Lifetime 87759-7
LOINC Code
| LOINC code | 87759-7 | ||
|---|---|---|---|
| name | Lifetime risk for developing genetic disease assessed Lifetime | ||
| description | The patient's ordinal risk (e.g. high/low) for developing a genetic disease in their lifetime. The likelihood may be based a number of factors, including family history (pedigree) analysis, genetic algorithm results, pre- or post-test results, and general population data for disease prevalence. | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Lifetime risk for developing genetic disease assessed | ||
| property | Likelihood | ||
| time | Lifetime | ||
| system | ^Patient | ||
| scale | Ord = Ordinal: Ordered categorical responses, e.g., 1+, 2+, 3+; positive, negative; reactive, indeterminate, nonreactive. | ||
| method | |||
Additional Names | |||
| short name | Lifetime Risk for genetic disease | ||
Basic Attributes | |||
| class | CLIN.RISK | ||
| type | 2 Clinical | ||
| order vs. observation | Both | ||
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 | 16512 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 | ||
| change reason | Release 2.67: TIME_ASPCT: Updated Timing to reflect the risk of developing a genetic disease in a lifetime. | ||
Related Names | |||
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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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