<?xml version="1.0"?>
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  <leader>00596nz  a2200217n  4500</leader>
  <controlfield tag="008">211208|||anznnbab||||||||||||||a|||||||d</controlfield>
  <datafield tag="024" ind1="8" ind2=" ">
    <subfield code="a">homoit0000044</subfield>
    <subfield code="0">https://homosaurus.org/v3/homoit0000044</subfield>
  </datafield>
  <datafield tag="040" ind1=" " ind2=" ">
    <subfield code="f">homoit</subfield>
  </datafield>
  <datafield tag="150" ind1=" " ind2=" ">
    <subfield code="a">Androgen insensitivity syndrome</subfield>
  </datafield>
  <datafield tag="450" ind1=" " ind2=" ">
    <subfield code="a">AIS</subfield>
  </datafield>
  <datafield tag="450" ind1=" " ind2=" ">
    <subfield code="a">Goldberg-Maxwell syndrome</subfield>
  </datafield>
  <datafield tag="450" ind1=" " ind2=" ">
    <subfield code="a">Male androgen insensitivity syndrome</subfield>
  </datafield>
  <datafield tag="550" ind1=" " ind2=" ">
    <subfield code="a">Variaciones intersex</subfield>
    <subfield code="0">https://homosaurus.org/v3/homoit0000669</subfield>
  </datafield>
  <datafield tag="680" ind1=" " ind2=" ">
    <subfield code="a">People born with AIS have XY chromosomes and testes, and their bodies have varying levels of insensitivity to androgens (including testosterone). This means that their cells do not respond typically to the testosterone that they produce. Like other variations in sex characteristics, AIS is a spectrum, with the subcategories of complete (CAIS), partial (PAIS), and mild androgen insensitivity (MAIS). The term "male androgen insensitivity syndrome" should not be used to describe this variation because many people with AIS are women.</subfield>
  </datafield>
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