<?xml version="1.0"?>
<record>
  <id>https://homosaurus.org/v3/homoit0000044</id>
  <identifier>homoit0000044</identifier>
  <prefLabel language="en">Androgen insensitivity syndrome</prefLabel>
  <altLabel language="en">AIS</altLabel>
  <altLabel language="en">Goldberg-Maxwell syndrome</altLabel>
  <altLabel language="en">Male androgen insensitivity syndrome</altLabel>
  <issued>
    <value>2019-05-14</value>
    <name>xsd:date</name>
  </issued>
  <modified>
    <value>2021-12-08</value>
    <name>xsd:date</name>
  </modified>
  <broader>
    <id>https://homosaurus.org/v3/homoit0000669</id>
    <prefLabel language="en">Intersex variations</prefLabel>
  </broader>
  <narrower>
    <id>https://homosaurus.org/v3/homoit0001079</id>
    <prefLabel language="en">Partial androgen insensitivity syndrome</prefLabel>
  </narrower>
  <narrower>
    <id>https://homosaurus.org/v3/homoit0002830</id>
    <prefLabel language="en">Complete gonadal dysgenesis</prefLabel>
  </narrower>
  <narrower>
    <id>https://homosaurus.org/v3/homoit0002866</id>
    <prefLabel language="en">Mild androgen insensitivity syndrome</prefLabel>
  </narrower>
  <comment language="en">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.</comment>
</record>
