<?xml version="1.0" encoding="utf-8" ?>
<?xml-stylesheet type="text/xsl" href="/efo/transforms/bioportal_bean.xsl"?>
<BioportalConcept>
  <label>Common variable agammaglobulinemia</label>
  <id>23238000</id>
  <fullId>http://purl.bioontology.org/ontology/SNOMEDCT/23238000</fullId>
  <synonyms>
    <string>Common variable immunodeficiency</string>
    <string>CVAG</string>
    <string>Acquired hypogammaglobulinaemia</string>
    <string>Acquired hypogammaglobulinemia</string>
    <string>CVI - Common variable immunodeficiency</string>
    <string>CVID - Common variable immunodeficiency</string>
    <string>Common variable hypogammaglobulinaemia</string>
    <string>Common variable hypogammaglobulinemia</string>
    <string>Late onset immunoglobulin deficiency</string>
    <string>Common variable agammaglobulinaemia</string>
    <string>Common variable agammaglobulinemia (disorder)</string>
  </synonyms>
  <relations>
    <BioportalEntry>
      <strings>
        <string>CONCEPTSTATUS</string>
      </strings>
      <list>
        <string>0</string>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>SubClass</string>
      </strings>
      <list>
        <BioportalConcept>
          <label>Common variable immunodeficiency with predominant immunoregulatory T-cell disorders</label>
          <id>191012007</id>
          <fullId>http://purl.bioontology.org/ontology/SNOMEDCT/191012007</fullId>
          <relations>
            <BioportalEntry>
              <strings>
                <string>CONCEPTSTATUS</string>
              </strings>
              <list>
                <string>0</string>
              </list>
            </BioportalEntry>
            <BioportalEntry>
              <strings>
                <string>ChildCount</string>
              </strings>
              <counter>0</counter>
            </BioportalEntry>
          </relations>
          <type>class</type>
        </BioportalConcept>
        <BioportalConcept>
          <label>Common variable immunodeficiency with autoantibodies to B- or T-cells</label>
          <id>191013002</id>
          <fullId>http://purl.bioontology.org/ontology/SNOMEDCT/191013002</fullId>
          <relations>
            <BioportalEntry>
              <strings>
                <string>CONCEPTSTATUS</string>
              </strings>
              <list>
                <string>0</string>
              </list>
            </BioportalEntry>
            <BioportalEntry>
              <strings>
                <string>ChildCount</string>
              </strings>
              <counter>0</counter>
            </BioportalEntry>
          </relations>
          <type>class</type>
        </BioportalConcept>
        <BioportalConcept>
          <label>Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions</label>
          <id>191011000</id>
          <fullId>http://purl.bioontology.org/ontology/SNOMEDCT/191011000</fullId>
          <relations>
            <BioportalEntry>
              <strings>
                <string>CONCEPTSTATUS</string>
              </strings>
              <list>
                <string>0</string>
              </list>
            </BioportalEntry>
            <BioportalEntry>
              <strings>
                <string>ChildCount</string>
              </strings>
              <counter>0</counter>
            </BioportalEntry>
          </relations>
          <type>class</type>
        </BioportalConcept>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>has_definitional_manifestation</string>
      </strings>
      <list>
        <BioportalConcept>
          <label>Immune system finding</label>
          <id>106182000</id>
          <fullId>http://purl.bioontology.org/ontology/SNOMEDCT/106182000</fullId>
          <relations>
            <BioportalEntry>
              <strings>
                <string>CONCEPTSTATUS</string>
              </strings>
              <list>
                <string>0</string>
              </list>
            </BioportalEntry>
            <BioportalEntry>
              <strings>
                <string>ChildCount</string>
              </strings>
              <counter>30</counter>
            </BioportalEntry>
          </relations>
          <type>class</type>
        </BioportalConcept>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>SNOMEDID</string>
      </strings>
      <list>
        <string>DC-51420</string>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>TUI</string>
      </strings>
      <list>
        <string>T047</string>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>same_as</string>
      </strings>
      <list>
        <BioportalConcept>
          <label>Common variable immunodeficiency</label>
          <id>191010004</id>
          <fullId>http://purl.bioontology.org/ontology/SNOMEDCT/191010004</fullId>
          <relations>
            <BioportalEntry>
              <strings>
                <string>CONCEPTSTATUS</string>
              </strings>
              <list>
                <string>2</string>
              </list>
            </BioportalEntry>
            <BioportalEntry>
              <strings>
                <string>ChildCount</string>
              </strings>
              <counter>0</counter>
            </BioportalEntry>
          </relations>
          <type>class</type>
        </BioportalConcept>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>CTV3ID</string>
      </strings>
      <list>
        <string>C3907</string>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>occurs_in</string>
      </strings>
      <list>
        <BioportalConcept>
          <label>Congenital</label>
          <id>255399007</id>
          <fullId>http://purl.bioontology.org/ontology/SNOMEDCT/255399007</fullId>
          <relations>
            <BioportalEntry>
              <strings>
                <string>CONCEPTSTATUS</string>
              </strings>
              <list>
                <string>0</string>
              </list>
            </BioportalEntry>
            <BioportalEntry>
              <strings>
                <string>ChildCount</string>
              </strings>
              <counter>0</counter>
            </BioportalEntry>
          </relations>
          <type>class</type>
        </BioportalConcept>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>SuperClass</string>
      </strings>
      <list>
        <BioportalConcept>
          <label>Congenital agammaglobulinemia</label>
          <id>116133005</id>
          <fullId>http://purl.bioontology.org/ontology/SNOMEDCT/116133005</fullId>
          <relations>
            <BioportalEntry>
              <strings>
                <string>CONCEPTSTATUS</string>
              </strings>
              <list>
                <string>0</string>
              </list>
            </BioportalEntry>
            <BioportalEntry>
              <strings>
                <string>ChildCount</string>
              </strings>
              <counter>5</counter>
            </BioportalEntry>
          </relations>
          <type>class</type>
        </BioportalConcept>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>has_clinical_course</string>
      </strings>
      <list>
        <BioportalConcept>
          <label>Courses</label>
          <id>288524001</id>
          <fullId>http://purl.bioontology.org/ontology/SNOMEDCT/288524001</fullId>
          <relations>
            <BioportalEntry>
              <strings>
                <string>CONCEPTSTATUS</string>
              </strings>
              <list>
                <string>0</string>
              </list>
            </BioportalEntry>
            <BioportalEntry>
              <strings>
                <string>ChildCount</string>
              </strings>
              <counter>7</counter>
            </BioportalEntry>
          </relations>
          <type>class</type>
        </BioportalConcept>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>SYNONYM PTGB</string>
      </strings>
      <list>
        <string>Common variable agammaglobulinaemia</string>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>ISPRIMITIVE</string>
      </strings>
      <list>
        <string>1</string>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>ChildCount</string>
      </strings>
      <counter>3</counter>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>SYNONYM SYGB</string>
      </strings>
      <list>
        <string>Acquired hypogammaglobulinaemia</string>
        <string>Common variable hypogammaglobulinaemia</string>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>Semantic_Type</string>
      </strings>
      <list>
        <string>Disease or Syndrome</string>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>isa</string>
      </strings>
      <list>
        <BioportalConcept>
          <label>Congenital agammaglobulinemia</label>
          <id>116133005</id>
          <fullId>http://purl.bioontology.org/ontology/SNOMEDCT/116133005</fullId>
          <relations>
            <BioportalEntry>
              <strings>
                <string>CONCEPTSTATUS</string>
              </strings>
              <list>
                <string>0</string>
              </list>
            </BioportalEntry>
            <BioportalEntry>
              <strings>
                <string>ChildCount</string>
              </strings>
              <counter>5</counter>
            </BioportalEntry>
          </relations>
          <type>class</type>
        </BioportalConcept>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>UMLS_CUI</string>
      </strings>
      <list>
        <string>C2936664</string>
        <string>C0009447</string>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>SYNONYM FN</string>
      </strings>
      <list>
        <string>Common variable agammaglobulinemia (disorder)</string>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>SYNONYM SY</string>
      </strings>
      <list>
        <string>Common variable immunodeficiency</string>
        <string>CVAG</string>
        <string>Acquired hypogammaglobulinemia</string>
        <string>CVI - Common variable immunodeficiency</string>
        <string>CVID - Common variable immunodeficiency</string>
        <string>Common variable hypogammaglobulinemia</string>
        <string>Late onset immunoglobulin deficiency</string>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>has_severity</string>
      </strings>
      <list>
        <BioportalConcept>
          <label>Severities</label>
          <id>272141005</id>
          <fullId>http://purl.bioontology.org/ontology/SNOMEDCT/272141005</fullId>
          <relations>
            <BioportalEntry>
              <strings>
                <string>CONCEPTSTATUS</string>
              </strings>
              <list>
                <string>0</string>
              </list>
            </BioportalEntry>
            <BioportalEntry>
              <strings>
                <string>ChildCount</string>
              </strings>
              <counter>7</counter>
            </BioportalEntry>
          </relations>
          <type>class</type>
        </BioportalConcept>
      </list>
    </BioportalEntry>
  </relations>
  <type>class</type>
</BioportalConcept>

