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_205.xml b/Rare diseases and classifications/Classifications of rare diseases/en_product3_205.xml
index 9a3fd5c..dd7dbc2 100644
--- a/Rare diseases and classifications/Classifications of rare diseases/en_product3_205.xml	
+++ b/Rare diseases and classifications/Classifications of rare diseases/en_product3_205.xml	
@@ -1,5 +1,5 @@
 <?xml version="1.0" encoding="ISO-8859-1"?>
-<JDBOR date="2024-07-01 09:25:07" 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 07:09:37" 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>
@@ -2348,7 +2348,7 @@
                           <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>
@@ -2360,7 +2360,7 @@
                           <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>
@@ -2398,7 +2398,7 @@
                       <Disorder id="390">
                         <OrphaCode>9</OrphaCode>
                         <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=9</ExpertLink>
-                        <Name lang="en">Tetrasomy X</Name>
+                        <Name lang="en">Tetrasomy X syndrome</Name>
                         <DisorderType id="21401">
                           <Name lang="en">Malformation syndrome</Name>
                         </DisorderType>
@@ -2422,7 +2422,7 @@
                       <Disorder id="1231">
                         <OrphaCode>3375</OrphaCode>
                         <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3375</ExpertLink>
-                        <Name lang="en">Trisomy X</Name>
+                        <Name lang="en">Trisomy X syndrome</Name>
                         <DisorderType id="21401">
                           <Name lang="en">Malformation syndrome</Name>
                         </DisorderType>
@@ -2554,7 +2554,7 @@
                       <Disorder id="12825">
                         <OrphaCode>96201</OrphaCode>
                         <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=96201</ExpertLink>
-                        <Name lang="en">X small rings</Name>
+                        <Name lang="en">X small rings syndrome</Name>
                         <DisorderType id="21401">
                           <Name lang="en">Malformation syndrome</Name>
                         </DisorderType>
@@ -2982,7 +2982,7 @@
                               <Disorder id="22720">
                                 <OrphaCode>398069</OrphaCode>
                                 <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=398069</ExpertLink>
-                                <Name lang="en">MAGEL2-related Prader-Willi-like syndrome</Name>
+                                <Name lang="en">Schaaf-Yang syndrome</Name>
                                 <DisorderType id="21394">
                                   <Name lang="en">Disease</Name>
                                 </DisorderType>
@@ -3788,7 +3788,7 @@
                           <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>
@@ -3800,7 +3800,7 @@
                           <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>
@@ -3838,7 +3838,7 @@
                       <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>
@@ -4054,7 +4054,7 @@
                       <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>