Personal Health Record System Functional Model, Release 2
0.1.0 - CI Build
Personal Health Record System Functional Model, Release 2 - Local Development build (v0.1.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
| Active as of 2024-01-31 |
<Requirements xmlns="http://hl7.org/fhir">
<id value="PHRSFMR2-PH.2.5.9"/>
<meta>
<profile value="http://hl7.org/ehrs/StructureDefinition/FMFunction"/>
</meta>
<text>
<status value="extensions"/>
<div xmlns="http://www.w3.org/1999/xhtml">
<table id="statements" class="grid dict">
<tr>
<td style="padding-left: 4px;">
<span>PH.2.5.9#01</span>
</td>
<td style="padding-left: 4px;">
<span>MAY</span>
</td>
<td style="padding-left: 4px;" class="requirement">
<span><div><p>The system MAY manage results of specific genetic tests, genetic markers, or findings according to user preference and/or consent, user role, organizational policy, and/or jurisdictional law.</p>
</div></span>
Satisfied by:<ol>
<li><a href="https://www.hl7.org/fhir/molecularsequence.html">https://www.hl7.org/fhir/molecularsequence.html</a></li>
</ol>
</td>
</tr>
<tr>
<td style="padding-left: 4px;">
<span>PH.2.5.9#02</span>
</td>
<td style="padding-left: 4px;">
<span>MAY</span>
</td>
<td style="padding-left: 4px;" class="requirement">
<span><div><p>The system MAY capture and present known genetically-based illnesses according to user preference and/or consent, user role, organizational policy, and/or jurisdictional law.</p>
</div></span>
</td>
</tr>
<tr>
<td style="padding-left: 4px;">
<span>PH.2.5.9#03</span>
</td>
<td style="padding-left: 4px;">
<span>MAY</span>
</td>
<td style="padding-left: 4px;" class="requirement">
<span><div><p>The system MAY capture and present a known single allele carrier status of a recessive genetic trait or diseases according to user preference and/or consent, user role, organizational policy, and/or jurisdictional law.</p>
</div></span>
</td>
</tr>
</table>
</div>
</text>
<url value="http://hl7.org/ehrs/Requirements/PHRSFMR2-PH.2.5.9"/>
<version value="0.1.0"/>
<name value="PH_2_5_9_Manage_Personal_Genetic_Information"/>
<title value="PH.2.5.9 Manage Personal Genetic Information (Function)"/>
<status value="active"/>
<date value="2024-01-31T14:45:34+00:00"/>
<publisher value="EHR WG"/>
<contact>
<telecom>
<system value="url"/>
<value value="http://www.hl7.org/Special/committees/ehr"/>
</telecom>
</contact>
<description
value="Limited personal genetic information is becoming available and it is anticipated that a much richer actionable data set will derive from current research. This function serves as a placeholder to take advantage of the scientific breakthroughs as they become available."/>
<statement>
<key value="PHRSFMR2-PH.2.5.9-01"/>
<label value="PH.2.5.9#01"/>
<conformance value="MAY"/>
<conditionality value="false"/>
<requirement
value="The system MAY manage results of specific genetic tests, genetic markers, or findings according to user preference and/or consent, user role, organizational policy, and/or jurisdictional law."/>
<satisfiedBy value="https://www.hl7.org/fhir/molecularsequence.html"/>
</statement>
<statement>
<key value="PHRSFMR2-PH.2.5.9-02"/>
<label value="PH.2.5.9#02"/>
<conformance value="MAY"/>
<conditionality value="false"/>
<requirement
value="The system MAY capture and present known genetically-based illnesses according to user preference and/or consent, user role, organizational policy, and/or jurisdictional law."/>
</statement>
<statement>
<key value="PHRSFMR2-PH.2.5.9-03"/>
<label value="PH.2.5.9#03"/>
<conformance value="MAY"/>
<conditionality value="false"/>
<requirement
value="The system MAY capture and present a known single allele carrier status of a recessive genetic trait or diseases according to user preference and/or consent, user role, organizational policy, and/or jurisdictional law."/>
</statement>
</Requirements>