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_201.xml b/Rare diseases and classifications/Classifications of rare diseases/en_product3_201.xml
index bc7abfe..cecf000 100644
--- a/Rare diseases and classifications/Classifications of rare diseases/en_product3_201.xml	
+++ b/Rare diseases and classifications/Classifications of rare diseases/en_product3_201.xml	
@@ -1,5 +1,5 @@
 <?xml version="1.0" encoding="ISO-8859-1"?>
-<JDBOR date="2024-07-01 09:24:41" 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 07:09:11" 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>
@@ -520,7 +520,7 @@
                                   <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>
@@ -1350,7 +1350,7 @@
                               <Disorder id="257">
                                 <OrphaCode>1646</OrphaCode>
                                 <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1646</ExpertLink>
-                                <Name lang="en">Chromosome Y microdeletion</Name>
+                                <Name lang="en">Chromosome Y microdeletion syndrome</Name>
                                 <DisorderType id="21401">
                                   <Name lang="en">Malformation syndrome</Name>
                                 </DisorderType>
@@ -1948,7 +1948,7 @@
                                   <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>
@@ -2120,7 +2120,7 @@
                           <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>
@@ -2132,7 +2132,7 @@
                           <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>
@@ -2204,7 +2204,7 @@
                           <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>
@@ -2264,7 +2264,7 @@
                           <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>
@@ -2276,7 +2276,7 @@
                           <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>