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    <Classification id="216">
      <OrphaNumber>168923</OrphaNumber>
      <Name lang="en">Orphanet classification of rare teratologic disorders</Name>
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            <OrphaCode>52662</OrphaCode>
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            <Name lang="en">Rare teratologic disease</Name>
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                <Name lang="en">Infectious embryofetopathy</Name>
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                    <Name lang="en">Fetal parvovirus syndrome</Name>
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                    <Name lang="en">Congenital rubella syndrome</Name>
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                    <Name lang="en">Congenital toxoplasmosis</Name>
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                    <Name lang="en">Congenital varicella syndrome</Name>
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                    <Name lang="en">Fetal cytomegalovirus syndrome</Name>
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                    <OrphaCode>292</OrphaCode>
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                    <Name lang="en">Congenital enterovirus infection</Name>
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                  <Disorder id="10967">
                    <OrphaCode>70596</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=70596</ExpertLink>
                    <Name lang="en">Congenital Epstein-Barr virus infection</Name>
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                      <Name lang="en">Disease</Name>
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                  <Disorder id="25941">
                    <OrphaCode>499009</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=499009</ExpertLink>
                    <Name lang="en">Congenital syphilis</Name>
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                      <Name lang="en">Disease</Name>
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                <OrphaCode>251529</OrphaCode>
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                <Name lang="en">Toxic or drug-related embryofetopathy</Name>
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                  <Name lang="en">Category</Name>
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                  <Disorder id="25307">
                    <OrphaCode>485358</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=485358</ExpertLink>
                    <Name lang="en">Propylthiouracil embryofetopathy</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                  <Disorder id="487">
                    <OrphaCode>1915</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1915</ExpertLink>
                    <Name lang="en">Fetal alcohol syndrome</Name>
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                      <Name lang="en">Malformation syndrome</Name>
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                    <OrphaCode>1908</OrphaCode>
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                    <Name lang="en">Aminopterin/methotrexate embryofetopathy</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                    <OrphaCode>1909</OrphaCode>
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                    <Name lang="en">Indomethacin embryofetopathy</Name>
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                      <Name lang="en">Malformation syndrome</Name>
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                    <OrphaCode>1910</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1910</ExpertLink>
                    <Name lang="en">Fetal iodine syndrome</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                    <OrphaCode>1911</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1911</ExpertLink>
                    <Name lang="en">Cocaine embryofetopathy</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
                    </DisorderType>
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                  <Disorder id="1874">
                    <OrphaCode>1918</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1918</ExpertLink>
                    <Name lang="en">Fetal minoxidil syndrome</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                  <Disorder id="1877">
                    <OrphaCode>1914</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1914</ExpertLink>
                    <Name lang="en">Vitamin K antagonist embryofetopathy</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                  <ClassificationNodeChildList count="0">
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                  <Disorder id="1879">
                    <OrphaCode>1916</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1916</ExpertLink>
                    <Name lang="en">Diethylstilbestrol syndrome</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
                    </DisorderType>
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                  <ClassificationNodeChildList count="0">
                  </ClassificationNodeChildList>
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                  <Disorder id="1880">
                    <OrphaCode>1917</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1917</ExpertLink>
                    <Name lang="en">Fetal methylmercury syndrome</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                    <OrphaCode>1920</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1920</ExpertLink>
                    <Name lang="en">Toluene embryopathy</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                    <OrphaCode>1923</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1923</ExpertLink>
                    <Name lang="en">Methimazole embryofetopathy</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                  <Disorder id="2166">
                    <OrphaCode>2305</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2305</ExpertLink>
                    <Name lang="en">Isotretinoin syndrome</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                  <Disorder id="2943">
                    <OrphaCode>3312</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=3312</ExpertLink>
                    <Name lang="en">Thalidomide embryopathy</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                  <ClassificationNodeChildList count="0">
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                  <Disorder id="10462">
                    <OrphaCode>40366</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=40366</ExpertLink>
                    <Name lang="en">Acitretin/etretinate embryopathy</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                <ClassificationNode>
                  <Disorder id="20172">
                    <OrphaCode>268249</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=268249</ExpertLink>
                    <Name lang="en">Mycophenolate mofetil embryopathy</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                  <Disorder id="22475">
                    <OrphaCode>370068</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=370068</ExpertLink>
                    <Name lang="en">Fetal anticonvulsant syndrome</Name>
                    <DisorderType id="21436">
                      <Name lang="en">Clinical group</Name>
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                      <Disorder id="1868">
                        <OrphaCode>1906</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1906</ExpertLink>
                        <Name lang="en">Fetal valproate spectrum disorder</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
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                      <Disorder id="1875">
                        <OrphaCode>1912</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1912</ExpertLink>
                        <Name lang="en">Fetal hydantoin syndrome</Name>
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                          <Name lang="en">Malformation syndrome</Name>
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                        <OrphaCode>1913</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1913</ExpertLink>
                        <Name lang="en">Fetal trimethadione syndrome</Name>
                        <DisorderType id="21401">
                          <Name lang="en">Malformation syndrome</Name>
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                      <Disorder id="1881">
                        <OrphaCode>1919</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1919</ExpertLink>
                        <Name lang="en">Phenobarbital embryopathy</Name>
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                          <Name lang="en">Malformation syndrome</Name>
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                      <Disorder id="22476">
                        <OrphaCode>370076</OrphaCode>
                        <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=370076</ExpertLink>
                        <Name lang="en">Fetal carbamazepine syndrome</Name>
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                          <Name lang="en">Malformation syndrome</Name>
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                <OrphaCode>251535</OrphaCode>
                <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=251535</ExpertLink>
                <Name lang="en">Maternal disease-related embryofetopathy</Name>
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                  <Name lang="en">Category</Name>
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                    <OrphaCode>1926</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=1926</ExpertLink>
                    <Name lang="en">Diabetic embryopathy</Name>
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                      <Name lang="en">Malformation syndrome</Name>
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                  <Disorder id="1889">
                    <OrphaCode>2209</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2209</ExpertLink>
                    <Name lang="en">Maternal phenylketonuria syndrome</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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                  <Disorder id="2093">
                    <OrphaCode>2216</OrphaCode>
                    <ExpertLink lang="en">http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&amp;Expert=2216</ExpertLink>
                    <Name lang="en">Maternal hyperthermia-induced birth defects</Name>
                    <DisorderType id="21401">
                      <Name lang="en">Malformation syndrome</Name>
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