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
CLIN; Diseases Hx Pnl; Fam Mem; Genetic diseases hx Pnl; Genetics; Genomic; Hx; Pan; PANEL.CLINICAL; Panl; Pnl; Point in time; Random
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