<?xml version="1.0" encoding="UTF-8"?>
<communities type="array">
  <community>
    <causes></causes>
    <created-at type="datetime">2008-10-23T16:14:10+00:00</created-at>
    <description>&lt;p&gt;Jacobsen Syndrome is a rare disorder resulting from deletion of a part of chromosome 11 causing mild mental retardation, a distinctive facial appearance, and various physical problems.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Jacobsen Syndrome is a rare disorder resulting from deletion of a part of chromosome 11 causing mild mental retardation, a distinctive facial appearance, and various physical problems.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">1225</id>
    <name>Jacobsen Syndrome</name>
    <participations-count type="integer">1</participations-count>
    <permalink>jacobsen-syndrome</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal" nil="true"></prevalence-number>
    <prevalence-number-source-url></prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>11q Deletion</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-09-21T19:33:40+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2009-11-09T14:04:08+00:00</created-at>
    <description>&lt;p&gt;Jarcho-Levin Syndrome is a rare hereditary skeletal growth disorder.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Jarcho-Levin Syndrome is a rare hereditary skeletal growth disorder.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">1448</id>
    <name>Jarcho-Levin Syndrome</name>
    <participations-count type="integer">0</participations-count>
    <permalink>jarcho-levin-syndrome</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal" nil="true"></prevalence-number>
    <prevalence-number-source-url></prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>Jarcho Levin Syndrome</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-11-09T14:04:08+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-11-09T15:01:52+00:00</created-at>
    <description>&lt;p&gt;Jejunal Atresia is a rare genetic disorder caused by the partial absence of the fold of the stomach membrane that connects the small intestine to the back wall of the abdomen resulting in the jejunal twisting around an artery of the colon.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Jejunal Atresia is a rare genetic disorder caused by the partial absence of the fold of the stomach membrane that connects the small intestine to the back wall of the abdomen resulting in the jejunal twisting around an artery of the colon.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms>&lt;p&gt;Symptoms include vomiting, a swollen abdomen, and constipation.&lt;/p&gt;</general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">1243</id>
    <name>Jejunal Atresia </name>
    <participations-count type="integer">7</participations-count>
    <permalink>jejunal-atresia</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal" nil="true"></prevalence-number>
    <prevalence-number-source-url></prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>Intestinal atresia, Apple Peel Syndrome, Christmas Tree Syndrome </synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">1</topics-count>
    <updated-at type="datetime">2009-07-30T10:40:56+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:35+00:00</created-at>
    <description></description>
    <diagnosis></diagnosis>
    <disorder-description></disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">981</id>
    <name>Jeune Syndrome</name>
    <participations-count type="integer">0</participations-count>
    <permalink>jeune-syndrome</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">0.2</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>Asphyxiating Thoracic Dystrophy </synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-06-11T22:17:01+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:34+00:00</created-at>
    <description>&lt;p&gt;Joubert Syndrome is a rare genetic disorder that affects the cerebellum, an area of the brain that controls balance and coordination.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Joubert Syndrome is a rare genetic disorder that affects the cerebellum, an area of the brain that controls balance and coordination.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">890</id>
    <name>Joubert Syndrome</name>
    <participations-count type="integer">1</participations-count>
    <permalink>joubert-syndrome</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">0.85</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags></synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2010-02-09T20:03:15+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:35+00:00</created-at>
    <description></description>
    <diagnosis></diagnosis>
    <disorder-description></disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">1025</id>
    <name>Junctional Epidermolysis Bullosa</name>
    <participations-count type="integer">0</participations-count>
    <permalink>junctional-epidermolysis-bullosa</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">0.06</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>EB</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-04-23T13:51:37+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:33+00:00</created-at>
    <description></description>
    <diagnosis></diagnosis>
    <disorder-description></disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">730</id>
    <name>Juvenile Psoriatic Arthritis</name>
    <participations-count type="integer">1</participations-count>
    <permalink>juvenile-psoriatic-arthritis</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">4.2</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags></synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-07T03:44:07+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:33+00:00</created-at>
    <description>&lt;p&gt;Juvenile X-Linked Retinoschisis is a rare genetic disorder primarily affecting young men.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Juvenile X-Linked Retinoschisis is a rare genetic disorder primarily affecting young men.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">725</id>
    <name>Juvenile X-Linked Retinoschisis</name>
    <participations-count type="integer">1</participations-count>
    <permalink>juvenile-x-linked-retinoschisis</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">4.5</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>X-Linked RS, Juvenile Retinoschisis, X Linked Retinoschisis, X-Linked Juvenile Retinoschisis, Juvenile X Linked Retinoschisis </synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-06T14:09:47+00:00</updated-at>
  </community>
</communities>
