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_200.xml b/Rare diseases and classifications/Classifications of rare diseases/en_product3_200.xml
index 0506270..01e5074 100644
--- a/Rare diseases and classifications/Classifications of rare diseases/en_product3_200.xml	
+++ b/Rare diseases and classifications/Classifications of rare diseases/en_product3_200.xml	
@@ -1,5 +1,5 @@
 <?xml version="1.0" encoding="ISO-8859-1"?>
-<JDBOR date="2024-07-01 09:24:36" 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 07:09:06" 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>
@@ -77,7 +77,7 @@
                       <Name lang="en">Category</Name>
                     </DisorderType>
                   </Disorder>
-                  <ClassificationNodeChildList count="185">
+                  <ClassificationNodeChildList count="188">
                     <ClassificationNode>
                       <Disorder id="27595">
                         <OrphaCode>529574</OrphaCode>
@@ -2694,6 +2694,42 @@
                       <ClassificationNodeChildList count="0">
                       </ClassificationNodeChildList>
                     </ClassificationNode>
+                    <ClassificationNode>
+                      <Disorder id="32151">
+                        <OrphaCode>684216</OrphaCode>
+                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=684216</ExpertLink>
+                        <Name lang="en">Intellectual disability-facial dysmorphism-joint hypermobility-hearing loss syndrome</Name>
+                        <DisorderType id="21401">
+                          <Name lang="en">Malformation syndrome</Name>
+                        </DisorderType>
+                      </Disorder>
+                      <ClassificationNodeChildList count="0">
+                      </ClassificationNodeChildList>
+                    </ClassificationNode>
+                    <ClassificationNode>
+                      <Disorder id="32193">
+                        <OrphaCode>688581</OrphaCode>
+                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=688581</ExpertLink>
+                        <Name lang="en">Midface hypoplasia-hearing impairment-elliptocytosis-nephrocalcinosis syndrome</Name>
+                        <DisorderType id="21401">
+                          <Name lang="en">Malformation syndrome</Name>
+                        </DisorderType>
+                      </Disorder>
+                      <ClassificationNodeChildList count="0">
+                      </ClassificationNodeChildList>
+                    </ClassificationNode>
+                    <ClassificationNode>
+                      <Disorder id="32195">
+                        <OrphaCode>688642</OrphaCode>
+                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=688642</ExpertLink>
+                        <Name lang="en">Turnpenny-Fry syndrome</Name>
+                        <DisorderType id="21401">
+                          <Name lang="en">Malformation syndrome</Name>
+                        </DisorderType>
+                      </Disorder>
+                      <ClassificationNodeChildList count="0">
+                      </ClassificationNodeChildList>
+                    </ClassificationNode>
                     <ClassificationNode>
                       <Disorder id="31898">
                         <OrphaCode>652532</OrphaCode>
@@ -2938,7 +2974,7 @@
                       <Disorder id="17027">
                         <OrphaCode>141064</OrphaCode>
                         <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=141064</ExpertLink>
-                        <Name lang="en">Lower lip fistula</Name>
+                        <Name lang="en">Isolated lower lip fistula</Name>
                         <DisorderType id="21415">
                           <Name lang="en">Morphological anomaly</Name>
                         </DisorderType>
@@ -3247,12 +3283,12 @@
                       </ClassificationNodeChildList>
                     </ClassificationNode>
                     <ClassificationNode>
-                      <Disorder id="418">
-                        <OrphaCode>1135</OrphaCode>
-                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1135</ExpertLink>
-                        <Name lang="en">Arrhinia-choanal atresia-microphthalmia syndrome</Name>
-                        <DisorderType id="21401">
-                          <Name lang="en">Malformation syndrome</Name>
+                      <Disorder id="2120">
+                        <OrphaCode>2250</OrphaCode>
+                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2250</ExpertLink>
+                        <Name lang="en">Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome</Name>
+                        <DisorderType id="21394">
+                          <Name lang="en">Disease</Name>
                         </DisorderType>
                       </Disorder>
                       <ClassificationNodeChildList count="0">
@@ -3797,7 +3833,7 @@
                       <Name lang="en">Category</Name>
                     </DisorderType>
                   </Disorder>
-                  <ClassificationNodeChildList count="3">
+                  <ClassificationNodeChildList count="4">
                     <ClassificationNode>
                       <Disorder id="26072">
                         <OrphaCode>502318</OrphaCode>
@@ -3810,6 +3846,18 @@
                       <ClassificationNodeChildList count="0">
                       </ClassificationNodeChildList>
                     </ClassificationNode>
+                    <ClassificationNode>
+                      <Disorder id="32181">
+                        <OrphaCode>686556</OrphaCode>
+                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=686556</ExpertLink>
+                        <Name lang="en">Isolated congenital cholesteatoma of the middle ear</Name>
+                        <DisorderType id="21415">
+                          <Name lang="en">Morphological anomaly</Name>
+                        </DisorderType>
+                      </Disorder>
+                      <ClassificationNodeChildList count="0">
+                      </ClassificationNodeChildList>
+                    </ClassificationNode>
                     <ClassificationNode>
                       <Disorder id="26069">
                         <OrphaCode>502305</OrphaCode>
@@ -4188,7 +4236,7 @@
                   <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>
@@ -4212,7 +4260,7 @@
                   <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>