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_185.xml b/Rare diseases and classifications/Classifications of rare diseases/en_product3_185.xml
index 359266f..f62e297 100644
--- a/Rare diseases and classifications/Classifications of rare diseases/en_product3_185.xml	
+++ b/Rare diseases and classifications/Classifications of rare diseases/en_product3_185.xml	
@@ -1,5 +1,5 @@
 <?xml version="1.0" encoding="ISO-8859-1"?>
-<JDBOR date="2024-07-01 09:23:15" 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 07:07:42" 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>
@@ -836,7 +836,7 @@
                           <Disorder id="14199">
                             <OrphaCode>99226</OrphaCode>
                             <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99226</ExpertLink>
-                            <Name lang="en">Monosomy X</Name>
+                            <Name lang="en">Monosomy X syndrome</Name>
                             <DisorderType id="21443">
                               <Name lang="en">Etiological subtype</Name>
                             </DisorderType>
@@ -848,7 +848,7 @@
                           <Disorder id="14200">
                             <OrphaCode>99228</OrphaCode>
                             <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99228</ExpertLink>
-                            <Name lang="en">Mosaic monosomy X</Name>
+                            <Name lang="en">Mosaic monosomy X syndrome</Name>
                             <DisorderType id="21443">
                               <Name lang="en">Etiological subtype</Name>
                             </DisorderType>
@@ -1844,7 +1844,7 @@
                           <Disorder id="334">
                             <OrphaCode>1642</OrphaCode>
                             <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1642</ExpertLink>
-                            <Name lang="en">Distal deletion 9p</Name>
+                            <Name lang="en">Distal deletion 9p syndrome</Name>
                             <DisorderType id="21401">
                               <Name lang="en">Malformation syndrome</Name>
                             </DisorderType>
@@ -2516,7 +2516,7 @@
                           <Disorder id="14199">
                             <OrphaCode>99226</OrphaCode>
                             <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99226</ExpertLink>
-                            <Name lang="en">Monosomy X</Name>
+                            <Name lang="en">Monosomy X syndrome</Name>
                             <DisorderType id="21443">
                               <Name lang="en">Etiological subtype</Name>
                             </DisorderType>
@@ -2528,7 +2528,7 @@
                           <Disorder id="14200">
                             <OrphaCode>99228</OrphaCode>
                             <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=99228</ExpertLink>
-                            <Name lang="en">Mosaic monosomy X</Name>
+                            <Name lang="en">Mosaic monosomy X syndrome</Name>
                             <DisorderType id="21443">
                               <Name lang="en">Etiological subtype</Name>
                             </DisorderType>
@@ -2602,7 +2602,7 @@
                       <Disorder id="18396">
                         <OrphaCode>199310</OrphaCode>
                         <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=199310</ExpertLink>
-                        <Name lang="en">Tetragametic chimerism</Name>
+                        <Name lang="en">Tetragametic chimerism syndrome</Name>
                         <DisorderType id="21401">
                           <Name lang="en">Malformation syndrome</Name>
                         </DisorderType>
@@ -2705,7 +2705,7 @@
                       <Name lang="en">Category</Name>
                     </DisorderType>
                   </Disorder>
-                  <ClassificationNodeChildList count="5">
+                  <ClassificationNodeChildList count="6">
                     <ClassificationNode>
                       <Disorder id="22309">
                         <OrphaCode>363478</OrphaCode>
@@ -2790,6 +2790,18 @@
                         </ClassificationNode>
                       </ClassificationNodeChildList>
                     </ClassificationNode>
+                    <ClassificationNode>
+                      <Disorder id="32163">
+                        <OrphaCode>685010</OrphaCode>
+                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=685010</ExpertLink>
+                        <Name lang="en">Mesothelioma of the tunica vaginalis</Name>
+                        <DisorderType id="21394">
+                          <Name lang="en">Disease</Name>
+                        </DisorderType>
+                      </Disorder>
+                      <ClassificationNodeChildList count="0">
+                      </ClassificationNodeChildList>
+                    </ClassificationNode>
                     <ClassificationNode>
                       <Disorder id="18502">
                         <OrphaCode>206484</OrphaCode>