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_182.xml b/Rare diseases and classifications/Classifications of rare diseases/en_product3_182.xml
index 9460451..2cac10f 100644
--- a/Rare diseases and classifications/Classifications of rare diseases/en_product3_182.xml	
+++ b/Rare diseases and classifications/Classifications of rare diseases/en_product3_182.xml	
@@ -1,5 +1,5 @@
 <?xml version="1.0" encoding="ISO-8859-1"?>
-<JDBOR date="2024-07-01 09:23:00" 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 07:07:27" 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>
@@ -103,7 +103,7 @@
                   <Name lang="en">Category</Name>
                 </DisorderType>
               </Disorder>
-              <ClassificationNodeChildList count="4">
+              <ClassificationNodeChildList count="5">
                 <ClassificationNode>
                   <Disorder id="11886">
                     <OrphaCode>88993</OrphaCode>
@@ -632,7 +632,7 @@
                           <Disorder id="337">
                             <OrphaCode>3378</OrphaCode>
                             <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3378</ExpertLink>
-                            <Name lang="en">Trisomy 13</Name>
+                            <Name lang="en">Trisomy 13 syndrome</Name>
                             <DisorderType id="21401">
                               <Name lang="en">Malformation syndrome</Name>
                             </DisorderType>
@@ -644,7 +644,7 @@
                           <Disorder id="339">
                             <OrphaCode>3380</OrphaCode>
                             <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3380</ExpertLink>
-                            <Name lang="en">Trisomy 18</Name>
+                            <Name lang="en">Trisomy 18 syndrome</Name>
                             <DisorderType id="21401">
                               <Name lang="en">Malformation syndrome</Name>
                             </DisorderType>
@@ -656,7 +656,7 @@
                           <Disorder id="557">
                             <OrphaCode>884</OrphaCode>
                             <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=884</ExpertLink>
-                            <Name lang="en">Tetrasomy 12p</Name>
+                            <Name lang="en">Tetrasomy 12p syndrome</Name>
                             <DisorderType id="21401">
                               <Name lang="en">Malformation syndrome</Name>
                             </DisorderType>
@@ -704,7 +704,7 @@
                           <Disorder id="1092">
                             <OrphaCode>1590</OrphaCode>
                             <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1590</ExpertLink>
-                            <Name lang="en">Distal deletion 13q</Name>
+                            <Name lang="en">Distal deletion 13q syndrome</Name>
                             <DisorderType id="21401">
                               <Name lang="en">Malformation syndrome</Name>
                             </DisorderType>
@@ -1004,7 +1004,7 @@
                           <Disorder id="12809">
                             <OrphaCode>96185</OrphaCode>
                             <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=96185</ExpertLink>
-                            <Name lang="en">Maternal uniparental disomy of chromosome 16</Name>
+                            <Name lang="en">Maternal uniparental disomy of chromosome 16 syndrome</Name>
                             <DisorderType id="21401">
                               <Name lang="en">Malformation syndrome</Name>
                             </DisorderType>
@@ -1347,19 +1347,7 @@
                           <Name lang="en">Category</Name>
                         </DisorderType>
                       </Disorder>
-                      <ClassificationNodeChildList count="9">
-                        <ClassificationNode>
-                          <Disorder id="17904">
-                            <OrphaCode>171220</OrphaCode>
-                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=171220</ExpertLink>
-                            <Name lang="en">Rectal duplication</Name>
-                            <DisorderType id="21415">
-                              <Name lang="en">Morphological anomaly</Name>
-                            </DisorderType>
-                          </Disorder>
-                          <ClassificationNodeChildList count="0">
-                          </ClassificationNodeChildList>
-                        </ClassificationNode>
+                      <ClassificationNodeChildList count="8">
                         <ClassificationNode>
                           <Disorder id="515">
                             <OrphaCode>2300</OrphaCode>
@@ -1446,7 +1434,7 @@
                               <Disorder id="32014">
                                 <OrphaCode>662480</OrphaCode>
                                 <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=662480</ExpertLink>
-                                <Name lang="en">Jujeno-ileal duplication</Name>
+                                <Name lang="en">Jejuno-ileal duplication</Name>
                                 <DisorderType id="21450">
                                   <Name lang="en">Clinical subtype</Name>
                                 </DisorderType>
@@ -1724,6 +1712,42 @@
                     </ClassificationNode>
                   </ClassificationNodeChildList>
                 </ClassificationNode>
+                <ClassificationNode>
+                  <Disorder id="32160">
+                    <OrphaCode>684757</OrphaCode>
+                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=684757</ExpertLink>
+                    <Name lang="en">Malformation of the anal canal and the rectum</Name>
+                    <DisorderType id="36561">
+                      <Name lang="en">Category</Name>
+                    </DisorderType>
+                  </Disorder>
+                  <ClassificationNodeChildList count="2">
+                    <ClassificationNode>
+                      <Disorder id="32159">
+                        <OrphaCode>684752</OrphaCode>
+                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=684752</ExpertLink>
+                        <Name lang="en">Isolated anal canal duplication</Name>
+                        <DisorderType id="21415">
+                          <Name lang="en">Morphological anomaly</Name>
+                        </DisorderType>
+                      </Disorder>
+                      <ClassificationNodeChildList count="0">
+                      </ClassificationNodeChildList>
+                    </ClassificationNode>
+                    <ClassificationNode>
+                      <Disorder id="17904">
+                        <OrphaCode>171220</OrphaCode>
+                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=171220</ExpertLink>
+                        <Name lang="en">Rectal duplication</Name>
+                        <DisorderType id="21415">
+                          <Name lang="en">Morphological anomaly</Name>
+                        </DisorderType>
+                      </Disorder>
+                      <ClassificationNodeChildList count="0">
+                      </ClassificationNodeChildList>
+                    </ClassificationNode>
+                  </ClassificationNodeChildList>
+                </ClassificationNode>
               </ClassificationNodeChildList>
             </ClassificationNode>
             <ClassificationNode>
@@ -1889,7 +1913,7 @@
                       <Name lang="en">Category</Name>
                     </DisorderType>
                   </Disorder>
-                  <ClassificationNodeChildList count="9">
+                  <ClassificationNodeChildList count="10">
                     <ClassificationNode>
                       <Disorder id="20908">
                         <OrphaCode>294415</OrphaCode>
@@ -2022,6 +2046,18 @@
                       <ClassificationNodeChildList count="0">
                       </ClassificationNodeChildList>
                     </ClassificationNode>
+                    <ClassificationNode>
+                      <Disorder id="32219">
+                        <OrphaCode>689829</OrphaCode>
+                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=689829</ExpertLink>
+                        <Name lang="en">Microphthalmia-motor delay-language delay-brain anomalies-diaphragmatic hernia syndrome</Name>
+                        <DisorderType id="21394">
+                          <Name lang="en">Disease</Name>
+                        </DisorderType>
+                      </Disorder>
+                      <ClassificationNodeChildList count="0">
+                      </ClassificationNodeChildList>
+                    </ClassificationNode>
                     <ClassificationNode>
                       <Disorder id="27458">
                         <OrphaCode>527468</OrphaCode>
@@ -2206,7 +2242,7 @@
                       <Disorder id="337">
                         <OrphaCode>3378</OrphaCode>
                         <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3378</ExpertLink>
-                        <Name lang="en">Trisomy 13</Name>
+                        <Name lang="en">Trisomy 13 syndrome</Name>
                         <DisorderType id="21401">
                           <Name lang="en">Malformation syndrome</Name>
                         </DisorderType>
@@ -2218,7 +2254,7 @@
                       <Disorder id="339">
                         <OrphaCode>3380</OrphaCode>
                         <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3380</ExpertLink>
-                        <Name lang="en">Trisomy 18</Name>
+                        <Name lang="en">Trisomy 18 syndrome</Name>
                         <DisorderType id="21401">
                           <Name lang="en">Malformation syndrome</Name>
                         </DisorderType>
@@ -2230,7 +2266,7 @@
                       <Disorder id="557">
                         <OrphaCode>884</OrphaCode>
                         <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=884</ExpertLink>
-                        <Name lang="en">Tetrasomy 12p</Name>
+                        <Name lang="en">Tetrasomy 12p syndrome</Name>
                         <DisorderType id="21401">
                           <Name lang="en">Malformation syndrome</Name>
                         </DisorderType>