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_187.xml b/Rare diseases and classifications/Classifications of rare diseases/en_product3_187.xml
index 4072fc9..f713597 100644
--- a/Rare diseases and classifications/Classifications of rare diseases/en_product3_187.xml	
+++ b/Rare diseases and classifications/Classifications of rare diseases/en_product3_187.xml	
@@ -1,5 +1,5 @@
 <?xml version="1.0" encoding="ISO-8859-1"?>
-<JDBOR date="2024-07-01 09:23:26" 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 07:07:53" 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>
@@ -4352,7 +4352,7 @@
                           <Disorder id="6520">
                             <OrphaCode>662</OrphaCode>
                             <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=662</ExpertLink>
-                            <Name lang="en">Yellow nail syndrome</Name>
+                            <Name lang="en">Lymphedema with yellow nails</Name>
                             <DisorderType id="21394">
                               <Name lang="en">Disease</Name>
                             </DisorderType>
@@ -4505,7 +4505,7 @@
                       <Name lang="en">Category</Name>
                     </DisorderType>
                   </Disorder>
-                  <ClassificationNodeChildList count="112">
+                  <ClassificationNodeChildList count="113">
                     <ClassificationNode>
                       <Disorder id="3069">
                         <OrphaCode>3200</OrphaCode>
@@ -6054,6 +6054,18 @@
                       <ClassificationNodeChildList count="0">
                       </ClassificationNodeChildList>
                     </ClassificationNode>
+                    <ClassificationNode>
+                      <Disorder id="32166">
+                        <OrphaCode>685067</OrphaCode>
+                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=685067</ExpertLink>
+                        <Name lang="en">Hypodontia-scalp hypotrichosis-facial dysmorphism syndrome</Name>
+                        <DisorderType id="21394">
+                          <Name lang="en">Disease</Name>
+                        </DisorderType>
+                      </Disorder>
+                      <ClassificationNodeChildList count="0">
+                      </ClassificationNodeChildList>
+                    </ClassificationNode>
                     <ClassificationNode>
                       <Disorder id="29437">
                         <OrphaCode>589608</OrphaCode>
@@ -9123,7 +9135,7 @@
                           <Name lang="en">Category</Name>
                         </DisorderType>
                       </Disorder>
-                      <ClassificationNodeChildList count="12">
+                      <ClassificationNodeChildList count="13">
                         <ClassificationNode>
                           <Disorder id="1007">
                             <OrphaCode>528</OrphaCode>
@@ -9352,6 +9364,18 @@
                           <ClassificationNodeChildList count="0">
                           </ClassificationNodeChildList>
                         </ClassificationNode>
+                        <ClassificationNode>
+                          <Disorder id="32182">
+                            <OrphaCode>686999</OrphaCode>
+                            <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=686999</ExpertLink>
+                            <Name lang="en">Lipodystrophy-demyelinating peripheral sensory-motor neuropathy syndrome</Name>
+                            <DisorderType id="21394">
+                              <Name lang="en">Disease</Name>
+                            </DisorderType>
+                          </Disorder>
+                          <ClassificationNodeChildList count="0">
+                          </ClassificationNodeChildList>
+                        </ClassificationNode>
                         <ClassificationNode>
                           <Disorder id="22331">
                             <OrphaCode>363649</OrphaCode>
@@ -9850,7 +9874,7 @@
                       <Disorder id="6520">
                         <OrphaCode>662</OrphaCode>
                         <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=662</ExpertLink>
-                        <Name lang="en">Yellow nail syndrome</Name>
+                        <Name lang="en">Lymphedema with yellow nails</Name>
                         <DisorderType id="21394">
                           <Name lang="en">Disease</Name>
                         </DisorderType>
@@ -10052,7 +10076,7 @@
                           <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>
@@ -10064,7 +10088,7 @@
                           <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>
@@ -11026,7 +11050,7 @@
                       <Disorder id="370">
                         <OrphaCode>626</OrphaCode>
                         <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=626</ExpertLink>
-                        <Name lang="en">Large congenital melanocytic nevus</Name>
+                        <Name lang="en">Large/giant congenital melanocytic nevus</Name>
                         <DisorderType id="21394">
                           <Name lang="en">Disease</Name>
                         </DisorderType>