Digital Transgender Archive

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  1. homosaurus/v4/homoit0002860

     
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    Description: Businesses owned by asexual people.@en

  2. homosaurus/v4/homoit0002861

     
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    Description: People with Jacobs syndrome develop with an extra Y chromosome. They might not have any obvious physical variations as a result, or they may be taller than usual or have other identifiable differen...

  3. homosaurus/v4/homoit0002862

     
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    Description: Kallmann syndrome can occur in people with XX or XY chromosomes and is a form of hypogonadism. People with Kallmann syndrome and XY chromosomes are often born with a smaller-than-typical penis and ...

  4. homosaurus/v4/homoit0002863

     
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    Description: People with Leydig cell hypoplasia (LCH) have XY chromosomes and a genetic insensitivity to luteinizing hormone. LCH can be either complete (known as LCH Type 1) or partial (known as LCH Type 2). L...

  5. homosaurus/v4/homoit0002864

     
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    Description: People with XY chromosomes and luteinizing hormone insensitivity develop the variation Leydig cell hypoplasiae. Because people with XX chromosomes do not typically produce Leydig cells to begin wit...

  6. homosaurus/v4/homoit0002865

     
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    Description: Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome occurs when a person's Müllerian ducts, which typically become the uterus and upper portion of the vagina during fetal development, do not develop in ...

  7. homosaurus/v4/homoit0002866

     
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    Description: People with mild androgen insensitivity syndrome (MAIS) respond to testosterone at a somewhat reduced level compared to typical levels, which means that they will usually be born with a penis (whic...

  8. homosaurus/v4/homoit0002867

     
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    Description: People with mixed gonadal dysgenesis are born with a mosaic (usually 45X/46XY) chromosome pattern and may develop some gonadal streak tissue and testicular tissue. They may be born with a vulva or ...

  9. homosaurus/v4/homoit0002868

     
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    Description: People with XX chromosomes can have a broad range of variations in how their Müllerian ducts (which typically form the uterus, fallopian tubes, cervix, and upper portion of the vagina) develop. The...

  10. homosaurus/v4/homoit0002869

     
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    Description: Non-classical congenital adrenal hyperplasia (CAH), a subtype of CAH, does not usually become apparent until later in childhood, adolescence, or even young adulthood.@en

  11. homosaurus/v4/homoit0002870

     
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    Description: People with penoscrotal transposition are born with a different genital configuration than typical, with their penis located below or in the middle of their scrotum instead of above it. Their scrot...

  12. homosaurus/v4/homoit0002871

     
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    Description: People with Persistent Müllerian duct syndrome (PMDS) have XY chromosomes, male-typical reproductive organs and external genitalia, and some component(s) of a female-typical reproductive tract, suc...

  13. homosaurus/v4/homoit0002872

     
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    Description: People with this variation have XX chromosomes and are generally born with a vulva and vagina, a uterus, and ovaries. Later in life, their ovaries often produce higher-than-typical levels of androg...

  14. homosaurus/v4/homoit0002873

     
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    Description: A term previously used in medical contexts to refer to different groups of intersex variations, usually divided into categories of “male pseudohermaphroditism” and “female pseudohermaphroditism” on...

  15. homosaurus/v4/homoit0002874

     
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    Description: People who have salt-wasting congenital adrenal hyperplasia (CAH), a subtype of classical CAH, experience "salt-wasting," a dangerous scenario a person's low levels of aldosterone cause their body ...