Genetic diseases history panel Family member HL7.VMR-CDS 74042-3
LOINC Code
| LOINC code | 74042-3 | ||
|---|---|---|---|
| name | Genetic diseases history panel Family member HL7.VMR-CDS | ||
| description | This panel is a subset of the Virtual Medical Record for Clinical Decision Support panel [LOINC: 74028-2]. It contains elements of the disease of interest, whether or not it is present and/or the cause of death in a family member, the family member's estimated age, and the genetic loci (gene identifier) of interest. This panel was created for, but not limited in use to, the Clinical Genomic Choice section in the HL7 v2 Implementation Guide for Virtual Medical Record (VMR). Note that VMR guide is different from the US Surgeon General family health portrait [LOINC: 54127-6], which is a public tool for users to document and share their family health history information. | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Genetic diseases history panel | ||
| property | - | ||
| 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 | ^Family member | ||
| scale | - | ||
| method | HL7.VMR-CDS | ||
Additional Names | |||
| short name | Genetic diseases hx Pnl Fam Mem VMR-CDS | ||
Basic Attributes | |||
| class | PANEL.CLIN | ||
| type | 2 Clinical | ||
| order vs. observation | Subset | ||
Panel Components | |||
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. | |||
Member of these Panels | |||
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History/Usage | |||
| first released | |||
| last updated | 2.48 | ||
| last change type | MIN - change to field other than name | ||
Related Names | |||
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