<?xml version="1.0" encoding="UTF-8"?>
<communities type="array">
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:34+00:00</created-at>
    <description>&lt;p&gt;Kabuki Syndrome is a very rare pediatric congenital disorder characterized by multiple congenital anomalies and mental retardation.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Kabuki Syndrome is a very rare pediatric congenital disorder characterized by multiple congenital anomalies and mental retardation.&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">848</id>
    <name>Kabuki Syndrome</name>
    <participations-count type="integer">1</participations-count>
    <permalink>kabuki-syndrome</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">1.16</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>Kabuki Makeup Syndrome, KMS, Niikawa Kuroki Syndrome</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-18T03:30:54+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">659</id>
    <name>Kallmann Syndrome</name>
    <participations-count type="integer">0</participations-count>
    <permalink>kallmann-syndrome</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">7.7</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>hypothalamic hypogonadism, familial hypogonadism with anosmia, hypogonadotropic hypogonadism</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-07-22T22:35:42+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;Kaposi&amp;#8217;s Sarcoma is a tumor caused by Human herpesvirus 8 (HHV8).&lt;/p&gt;</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">825</id>
    <name>Kaposi's Sarcoma</name>
    <participations-count type="integer">0</participations-count>
    <permalink>kaposi-s-sarcoma</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">1.7</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>Kaposis sarcoma, KS, Kaposi's sarcoma-associated herpesvirus, Kaposis sarcoma-associated herpesvirus </synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-07-27T23:01:39+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2009-01-02T22:26:34+00:00</created-at>
    <description>&lt;p&gt;Kawasaki Disease is a rare form of  vasculitis characterized by high fevers, rash, swelling of lymph nodes in the neck and pain.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Kawasaki Disease is a rare form of  vasculitis characterized by high fevers, rash, swelling of lymph nodes in the neck and pain.&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">1305</id>
    <name>Kawasaki Disease</name>
    <participations-count type="integer">0</participations-count>
    <permalink>kawasaki-disease</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>Mucocutaneous Lymph Node Syndrome, MLNS, Infantile Polyarteritis, Kawasaki Syndrome, KD</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-01-02T22:26:34+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;Kearns-Sayre Syndrome is a rare disorder caused by a 5,000 base deletion in the mitochondrial &lt;span class="caps"&gt;DNA&lt;/span&gt;.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Kearns-Sayre Syndrome is a rare disorder caused by a 5,000 base deletion in the mitochondrial &lt;span class="caps"&gt;DNA&lt;/span&gt;.&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">804</id>
    <name>Kearns-Sayre Syndrome</name>
    <participations-count type="integer">2</participations-count>
    <permalink>kearns-sayre-syndrome</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">2.0</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>Ragged Red Fiber Myopathy, Oculocraniosomatic Syndrome, KSS, Mitochondrial Myopathy, Kearns Sayre Syndrome</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">1</topics-count>
    <updated-at type="datetime">2009-08-05T03:12:22+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;Kennedy&amp;#8217;s Disease is a rare neuromuscular disease involving the mutation of the androgen receptor.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Kennedy&amp;#8217;s Disease is a rare neuromuscular disease involving the mutation of the androgen receptor.&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">775</id>
    <name>Kennedy's Disease</name>
    <participations-count type="integer">0</participations-count>
    <permalink>kennedy-s-disease</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">2.8</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>Kennedy disease Kennedys disease, KD, X-linked spinal and bulbar muscular atrophy, SBMA, spinobulbar muscular atrophy, X-Linked bulbo-spinal atrophy</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2010-01-30T22:41:57+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2009-04-29T13:53:24+00:00</created-at>
    <description>&lt;p&gt;Keratoconus is an eye disorder in which structural changes within the cornea cause it to thin and become more conical.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Keratoconus is an eye disorder in which structural changes within the cornea cause it to thin and become more conical.&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">1379</id>
    <name>Keratoconus</name>
    <participations-count type="integer">0</participations-count>
    <permalink>keratoconus</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></synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-04-29T13:53:24+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-06-02T17:37:09+00:00</created-at>
    <description>&lt;p&gt;Kienbock&amp;#8217;s disease is a wrist disorder caused by the breakdown of the lunate bone.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Kienbock&amp;#8217;s disease is a wrist disorder caused by the breakdown of the lunate bone.&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">1108</id>
    <name>Kienbock's Disease</name>
    <participations-count type="integer">3</participations-count>
    <permalink>kienbock-s-disease</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>Kienbocks Disease, avascular necrosis</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-09-25T13:47:37+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-07-23T17:45:08+00:00</created-at>
    <description>&lt;p&gt;Kikuchi&amp;#8217;s disease is a rare non-cancerous enlargement of the lymph nodes.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Kikuchi&amp;#8217;s disease is a rare non-cancerous enlargement of the lymph nodes.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms>&lt;p&gt;swollen lymph nodes, fever&lt;/p&gt;</general-symptoms>
    <general-test>&lt;p&gt;lymph node biopsy&lt;/p&gt;</general-test>
    <general-treatment></general-treatment>
    <id type="integer">1188</id>
    <name>Kikuchi's Disease </name>
    <participations-count type="integer">2</participations-count>
    <permalink>kikuchi-s-disease</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>KD, Histiocytic necrotizing lymphadenitis, Kikuchis Disease </synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-05T03:11:33+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-26T00:01:30+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">1081</id>
    <name>Klatskin Tumor</name>
    <participations-count type="integer">0</participations-count>
    <permalink>klatskin-tumor</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>Hilar Cholangiocarcinoma, Klatskin Tumour, Klatskins Tumor</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-06-03T18:27:49+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-07-05T17:47:14+00:00</created-at>
    <description>&lt;p&gt;Kleine-Levin Syndrome is a rare disorder characterized by the need for excessive amounts of sleep.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Kleine-Levin Syndrome is a rare disorder characterized by the need for excessive amounts of sleep.&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">1139</id>
    <name>Kleine-Levin Syndrome</name>
    <participations-count type="integer">3</participations-count>
    <permalink>kleine-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>KLS, Hybernation Syndrome, Kleine Levin Syndrome</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-05T03:13:25+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-10-21T18:39:03+00:00</created-at>
    <description>&lt;p&gt;Klinefelter&amp;#8217;s Syndrome is a rare genetic condition caused by a chromosome aneuploidy.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Klinefelter&amp;#8217;s Syndrome is a rare genetic condition caused by a chromosome aneuploidy.&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">1221</id>
    <name>Klinefelter's Syndrome</name>
    <participations-count type="integer">5</participations-count>
    <permalink>klinefelter-s-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>Klinefelter Syndrome, 47,XXY, XXY Syndrome, XXXY Syndrome, Klinefelters Syndrome</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">1</topics-count>
    <updated-at type="datetime">2008-12-11T01:15:01+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;Klippel-Feil Syndrome is a rare disorder characterized by the fusion of any 2 of the 7 cervical vertebrae.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Klippel-Feil Syndrome is a rare disorder characterized by the fusion of any 2 of the 7 cervical vertebrae.&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">805</id>
    <name>Klippel-Feil Syndrome</name>
    <participations-count type="integer">1</participations-count>
    <permalink>klippel-feil-syndrome</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">2.0</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>Klippel Feil Syndrome</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-03T03:14:15+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-07-05T18:52:27+00:00</created-at>
    <description>&lt;p&gt;Klippel-Trenaunay Syndrome is a congenital circulatory disorder characterized by hemiangiomas, arteriovenous abscesses, and varicose veins, usually on the limbs.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Klippel-Trenaunay Syndrome is a congenital circulatory disorder characterized by hemiangiomas, arteriovenous abscesses, and varicose veins, usually on the limbs.&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">1144</id>
    <name>Klippel-Trenaunay Syndrome</name>
    <participations-count type="integer">3</participations-count>
    <permalink>klippel-trenaunay-syndrome</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">1000.0</prevalence-number>
    <prevalence-number-source-url>http://www.chestjournal.org/content/115/4/1199.full</prevalence-number-source-url>
    <prevalence-type>Cases</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>KTS, Klippel-Tr&#233;naunay-Weber Syndrome, Klippel Trenaunay Weber Syndrome, Klippel-Tr&#233;naunay syndrome, KTWS, Klippel Trenaunay Syndrome </synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-04T14:30:56+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;Krabbe Disease is a rare disorder that affects the myelin sheath of the nervous system.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Krabbe Disease is a rare disorder that affects the myelin sheath of the nervous system.&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">899</id>
    <name>Krabbe Disease</name>
    <participations-count type="integer">0</participations-count>
    <permalink>krabbe-disease</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">0.75</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>globoid cell leukodystrophy, galactosylceramide lipidosis, Subset of Lysosomal Storage Disease  </synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2010-02-09T22:54:42+00:00</updated-at>
  </community>
</communities>
