commit 6eb274384f0c4cd30cc83f08ce097956913930ce
Author: davidlagorce <david.lagorce@inserm.fr>
Date:   Wed Dec 4 08:42:13 2024 +0100

    DEC 2024

diff --git a/Rare diseases and classifications/Classifications of rare diseases/en_product3_194.xml b/Rare diseases and classifications/Classifications of rare diseases/en_product3_194.xml
index 4ec3810..cb603cc 100644
--- a/Rare diseases and classifications/Classifications of rare diseases/en_product3_194.xml	
+++ b/Rare diseases and classifications/Classifications of rare diseases/en_product3_194.xml	
@@ -1,5 +1,5 @@
 <?xml version="1.0" encoding="ISO-8859-1"?>
-<JDBOR date="2024-07-01 09:23:59" version="1.3.29 / 4.1.7 [2023-08-02] (orientdb version)" copyright="Orphanet (c) 2024" dbserver="jdbc:sybase:Tds:canard.orpha.net:2020">
+<JDBOR date="2024-12-03 07:08:29" version="1.3.29 / 4.1.7 [2023-08-02] (orientdb version)" copyright="Orphanet (c) 2024" dbserver="jdbc:sybase:Tds:canard.orpha.net:2020">
   <Availability> 
     <Licence>
       <FullName lang="en">Creative Commons Attribution 4.0 International</FullName>
@@ -1547,7 +1547,55 @@
                                   <Name lang="en">Disease</Name>
                                 </DisorderType>
                               </Disorder>
-                              <ClassificationNodeChildList count="0">
+                              <ClassificationNodeChildList count="4">
+                                <ClassificationNode>
+                                  <Disorder id="32186">
+                                    <OrphaCode>687733</OrphaCode>
+                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=687733</ExpertLink>
+                                    <Name lang="en">Pulmonary Langerhans cell histiocytosis</Name>
+                                    <DisorderType id="21450">
+                                      <Name lang="en">Clinical subtype</Name>
+                                    </DisorderType>
+                                  </Disorder>
+                                  <ClassificationNodeChildList count="0">
+                                  </ClassificationNodeChildList>
+                                </ClassificationNode>
+                                <ClassificationNode>
+                                  <Disorder id="32188">
+                                    <OrphaCode>687741</OrphaCode>
+                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=687741</ExpertLink>
+                                    <Name lang="en">Multisystem Langerhans cell histiocytosis</Name>
+                                    <DisorderType id="21450">
+                                      <Name lang="en">Clinical subtype</Name>
+                                    </DisorderType>
+                                  </Disorder>
+                                  <ClassificationNodeChildList count="0">
+                                  </ClassificationNodeChildList>
+                                </ClassificationNode>
+                                <ClassificationNode>
+                                  <Disorder id="32187">
+                                    <OrphaCode>687738</OrphaCode>
+                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=687738</ExpertLink>
+                                    <Name lang="en">Single-system multifocal Langerhans cell histiocytosis</Name>
+                                    <DisorderType id="21450">
+                                      <Name lang="en">Clinical subtype</Name>
+                                    </DisorderType>
+                                  </Disorder>
+                                  <ClassificationNodeChildList count="0">
+                                  </ClassificationNodeChildList>
+                                </ClassificationNode>
+                                <ClassificationNode>
+                                  <Disorder id="32185">
+                                    <OrphaCode>687730</OrphaCode>
+                                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=687730</ExpertLink>
+                                    <Name lang="en">Unifocal Langerhans cell histiocytosis</Name>
+                                    <DisorderType id="21450">
+                                      <Name lang="en">Clinical subtype</Name>
+                                    </DisorderType>
+                                  </Disorder>
+                                  <ClassificationNodeChildList count="0">
+                                  </ClassificationNodeChildList>
+                                </ClassificationNode>
                               </ClassificationNodeChildList>
                             </ClassificationNode>
                             <ClassificationNode>
@@ -5991,7 +6039,7 @@
                           <Name lang="en">Category</Name>
                         </DisorderType>
                       </Disorder>
-                      <ClassificationNodeChildList count="6">
+                      <ClassificationNodeChildList count="7">
                         <ClassificationNode>
                           <Disorder id="28857">
                             <OrphaCode>576742</OrphaCode>
@@ -6064,6 +6112,18 @@
                             </ClassificationNode>
                           </ClassificationNodeChildList>
                         </ClassificationNode>
+                        <ClassificationNode>
+                          <Disorder id="32193">
+                            <OrphaCode>688581</OrphaCode>
+                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=688581</ExpertLink>
+                            <Name lang="en">Midface hypoplasia-hearing impairment-elliptocytosis-nephrocalcinosis syndrome</Name>
+                            <DisorderType id="21401">
+                              <Name lang="en">Malformation syndrome</Name>
+                            </DisorderType>
+                          </Disorder>
+                          <ClassificationNodeChildList count="0">
+                          </ClassificationNodeChildList>
+                        </ClassificationNode>
                         <ClassificationNode>
                           <Disorder id="413">
                             <OrphaCode>1046</OrphaCode>