<?xml version="1.0" encoding="UTF-8"?>
<communities type="array">
  <community>
    <causes></causes>
    <created-at type="datetime">2009-08-20T12:16:25+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">1430</id>
    <name>Aagenaes Syndrome</name>
    <participations-count type="integer">0</participations-count>
    <permalink>aagenaes-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>cholestasis-lymphedema syndrome, CLS, cholestasis lymphedema syndrome</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-09-17T22:19:36+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-10-24T20:35:26+00:00</created-at>
    <description>&lt;p&gt;Aarskog-Scott Syndrome is a rare genetic disease characterized by short stature, facial abnormalities, skeletal and genital anomalies.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Aarskog-Scott Syndrome is a rare genetic disease characterized by short stature, facial abnormalities, skeletal and genital anomalies.&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">1228</id>
    <name>Aarskog-Scott Syndrome </name>
    <participations-count type="integer">0</participations-count>
    <permalink>aarskog-scott-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>Aarskog Syndrome, AAS, Faciodigitogenital Syndrome, Shawl Scrotum Syndrome, Faciogenital Dysplasia, Aarskog Scott Syndrome 
</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-07-31T21:18:47+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2009-08-19T20:47:07+00:00</created-at>
    <description>&lt;p&gt;Aase Syndrome is a rare inherited disorder characterized by anemia with some joint and skeletal deformities.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Aase Syndrome is a rare inherited disorder characterized by anemia with some joint and skeletal deformities.&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">1413</id>
    <name>Aase Syndrome </name>
    <participations-count type="integer">0</participations-count>
    <permalink>aase-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>Aase-Smith Syndrome, Aase Smith Syndrome </synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-19T21:01:31+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;Acalvaria is a rare malformation characterized by the absence of the calvarial bones, dura mater and associated muscles in the presence of a normal skull base and normal facial bones.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Acalvaria is a rare malformation characterized by absence of the calvarial bones, dura mater and associated muscles in the presence of a normal skull base and normal facial bones.&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">886</id>
    <name>Acalvaria</name>
    <participations-count type="integer">2</participations-count>
    <permalink>acalvaria</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">1.0</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>Acrania, Congenital Malformation</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-02-10T14:42:15+00:00</updated-at>
  </community>
  <community>
    <causes>&lt;p&gt;Causes include using contaminated water on contact lenses, using homemade solutions to store and clean contacts, wearing contact lenses in a hot tub and swimming or showering while wearing lenses.&lt;/p&gt;</causes>
    <created-at type="datetime">2008-05-21T13:25:34+00:00</created-at>
    <description>&lt;p&gt;Acanthamoeba Keratitis is a rare eye infection resulting from an amoeba that is most commonly associated with incorrect contact lens handling and exposure to unsanitary conditions.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Acanthamoeba Keratitis is a rare eye infection resulting from an amoeba that is most commonly associated with incorrect contact lens handling and exposure to unsanitary conditions.&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">856</id>
    <name>Acanthamoeba Keratitis</name>
    <participations-count type="integer">22</participations-count>
    <permalink>acanthamoeba-keratitis</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">1.0</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></synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">1</topics-count>
    <updated-at type="datetime">2008-12-27T05:56:31+00:00</updated-at>
  </community>
  <community>
    <causes>&lt;p&gt;Genetic&lt;/p&gt;</causes>
    <created-at type="datetime">2008-05-21T13:25:34+00:00</created-at>
    <description>&lt;p&gt;Acatalasemia a genetic deficiency of erythrocyte catalase characterized by infection of the gums.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Acatalasemia a genetic deficiency of erythrocyte catalase characterized by infection of the gums.&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">766</id>
    <name>Acatalasemia</name>
    <participations-count type="integer">0</participations-count>
    <permalink>acatalasemia</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">3.1</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>Acatalasia, Takahara's disease, Takaharas disease</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">1</topics-count>
    <updated-at type="datetime">2009-09-17T22:46:26+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:35+00:00</created-at>
    <description>&lt;p&gt;Aceruloplasminemia is a rare iron metabolism disorder characterized by progressive neurodegeneration of the retina and basal ganglia, and diabetes mellitus.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Aceruloplasminemia is a rare iron metabolism disorder characterized by progressive neurodegeneration of the retina and basal ganglia, and diabetes mellitus.&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">1027</id>
    <name>Aceruloplasminemia</name>
    <participations-count type="integer">1</participations-count>
    <permalink>aceruloplasminemia</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">0.05</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>Neurodegeneration with Brain Iron Accumulation, NBIA</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2010-01-24T18:58:44+00:00</updated-at>
  </community>
  <community>
    <causes>&lt;p&gt;The official cause of Achalasia is unknown, but it is believed to be caused by infection, heredity or an autoimmune disease.&lt;/p&gt;</causes>
    <created-at type="datetime">2008-07-14T22:56:55+00:00</created-at>
    <description>&lt;p&gt;Achalasia is a rare disorder affecting the lower esophageal sphincter characterized by difficulty in swallowing (dysphagia) and regurgitation of undigested food.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Achalasia is a rare disorder affecting the lower esophageal sphincter characterized by difficulty in swallowing (dysphagia) and regurgitation of undigested food.&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">1174</id>
    <name>Achalasia</name>
    <participations-count type="integer">6</participations-count>
    <permalink>achalasia</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">8.0</prevalence-number>
    <prevalence-number-source-url>http://www.coughjournal.com/content/4/1/6</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>Esophageal Achalasia, Achalasia Cardiae, Cardiospasm, Dyssynergia Esophagus, Esophageal Aperistalsis, primary achalasia</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2010-02-09T17:13:02+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2009-08-19T22:32:20+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">1427</id>
    <name>Acheiropodia</name>
    <participations-count type="integer">0</participations-count>
    <permalink>acheiropodia</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>Horn Kolb Syndrome, Acheiropody, Aleijadinhos</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-19T22:32:20+00:00</updated-at>
  </community>
  <community>
    <causes nil="true"></causes>
    <created-at type="datetime">2008-05-21T13:25:33+00:00</created-at>
    <description nil="true"></description>
    <diagnosis nil="true"></diagnosis>
    <disorder-description nil="true"></disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms nil="true"></general-symptoms>
    <general-test nil="true"></general-test>
    <general-treatment nil="true"></general-treatment>
    <id type="integer">723</id>
    <name>Achondroplasia</name>
    <participations-count type="integer">1</participations-count>
    <permalink>achondroplasia</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 nil="true"></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags nil="true"></synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">2</topics-count>
    <updated-at type="datetime">2009-05-04T09:53:03+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2009-08-20T12:20:31+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">1431</id>
    <name>Ackerman Syndrome </name>
    <participations-count type="integer">0</participations-count>
    <permalink>ackerman-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>interstitial granulomatous dermatitis</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-20T12:20:31+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-07-08T04:25:33+00:00</created-at>
    <description>&lt;p&gt;Acoustic neuroma is a benign tumor that forms on the vestibulocochlear nerve leading from the brain to the inner ear.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Acoustic neuroma is a benign tumor that forms on the vestibulocochlear nerve leading from the brain to the inner ear.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms>&lt;p&gt;Hearing loss &lt;br /&gt;
Ringing in the ears (tinnitus) &lt;br /&gt;
Dizziness (vertigo) &lt;br /&gt;
Difficulty in balance (imbalance or dysequilibrium) &lt;br /&gt;
Fullness or pressure in the ears &lt;br /&gt;
Facial numbness or paralysis (for very large tumors)&lt;/p&gt;</general-symptoms>
    <general-test></general-test>
    <general-treatment>&lt;p&gt;Radiation, Surgery&lt;/p&gt;</general-treatment>
    <id type="integer">1151</id>
    <name>Acoustic Neuroma</name>
    <participations-count type="integer">1</participations-count>
    <permalink>acoustic-neuroma</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>Vestibular schwannoma, Neurolemmoma</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2008-09-02T15:11:07+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">1013</id>
    <name>Acquired Hemophilia</name>
    <participations-count type="integer">1</participations-count>
    <permalink>acquired-hemophilia</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">0.1</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">2009-07-02T18:34:27+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">975</id>
    <name>Acrodermatitis Enteropathica</name>
    <participations-count type="integer">0</participations-count>
    <permalink>acrodermatitis-enteropathica</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>Zinc deficiency, Brandt Syndrome 
Danbolt-Cross Syndrome,
Congenital Zinc deficiency, AEZ</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-02-19T19:55:23+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-25T23:12:18+00:00</created-at>
    <description>&lt;p&gt;Acrofacial Dysostosis is a group of disorders characterized by defective limb and facial development.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Acrofacial Dysostosis is a group of disorders characterized by defective limb and facial development.&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">1067</id>
    <name>Acrofacial Dysostosis, Rodriguez Type</name>
    <participations-count type="integer">1</participations-count>
    <permalink>acrofacial-dysostosis--rodriguez-type</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>Acrofacial Syndrome</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2008-12-07T04:37:15+00:00</updated-at>
  </community>
</communities>
