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_209.xml b/Rare diseases and classifications/Classifications of rare diseases/en_product3_209.xml
index 21bf170..b4aa653 100644
--- a/Rare diseases and classifications/Classifications of rare diseases/en_product3_209.xml	
+++ b/Rare diseases and classifications/Classifications of rare diseases/en_product3_209.xml	
@@ -1,5 +1,5 @@
 <?xml version="1.0" encoding="ISO-8859-1"?>
-<JDBOR date="2024-07-01 09:25:13" 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 07:09:42" 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>
@@ -1104,7 +1104,7 @@
                   <Disorder id="330">
                     <OrphaCode>1600</OrphaCode>
                     <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1600</ExpertLink>
-                    <Name lang="en">Monosomy 18q</Name>
+                    <Name lang="en">Monosomy 18q syndrome</Name>
                     <DisorderType id="21401">
                       <Name lang="en">Malformation syndrome</Name>
                     </DisorderType>
@@ -1128,7 +1128,7 @@
                   <Disorder id="562">
                     <OrphaCode>718</OrphaCode>
                     <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=718</ExpertLink>
-                    <Name lang="en">Isolated Pierre Robin syndrome</Name>
+                    <Name lang="en">Isolated Pierre Robin sequence</Name>
                     <DisorderType id="21401">
                       <Name lang="en">Malformation syndrome</Name>
                     </DisorderType>