Swyer syndrome, also known as complete gonadal dysgenesis or XY gonadal dysgenesis, is a rare condition that affects about 1 in 80,000 births.
Androgen insensitivity syndrome (AIS) is a rare genetic condition that affects how the body uses male hormones during fetal development and after birth. It can occur in both males and females, and there are different types of AIS with varying degrees of severity:
Complete AIS: Affects 2–5 in 100,000 female infants assigned male at birth. In this form, the body doesn't respond to androgens at all, so children develop as females but lack internal reproductive organs.
Partial AIS: Affects 1 in 99,000 male infants. This type of AIS is very rare in the general population, but females can be carriers.
Mild AIS: Much less common than complete and partial AIS.
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome affects about 1 in 4,500 to 5,000 female newborns. MRKH syndrome is the second most common cause of primary amenorrhea. It's usually diagnosed around age 15 if a child has not started their period. The first symptom is usually amenorrhea, but young women with MRKH may otherwise have normal development of secondary sexual characteristics and normal external genitalia.
Persistent Müllerian Duct Syndrome (PMDS) is a rare disorder of sexual differentiation (DSD), also known as intersex, that affects males and is characterized by the presence of female reproductive systems. As of October 2019, there were fewer than 300 reported cases worldwide.
Ovotesticular disorder of sex development (OT-DSD), also known as "true hermaphroditism," is a rare condition that affects less than 1 in 20,000 births. It may account for less than 3–10% of all disorders of sex development (DSD).
5-alpha reductase deficiency (5-αRD) is a rare congenital disorder whose exact incidence is unknown. However, some evidence suggests it's more common in certain countries, including the Dominican Republic, Papua New Guinea, Turkey, and Egypt. In the Dominican Republic, the condition has a high prevalence due to the large number of consanguineous marriages. A 2020 study found 434 cases of 5-αRD across 44 countries, including Turkey (23%), China (17%), Italy (9%), and Brazil (7%). 5-αRD is also rare in white people.
Ambiguous genitalia, also known as atypical genitalia, is a rare birth defect that affects about 1 in 4,500 to 5,000 live births. It occurs when a baby's external genitals are not clearly male or female or when the genitals are not well formed. The baby may have characteristics of both sexes, or the outer genitalia may not match the internal sex organs.
"Women who get hysterectomies" you literally just said only women (humans with a uterus) get this procedure.
Genital mutilation in women (you know humans with a clitorious?) is only of that one specific organ. They would still have a uterus and ovaries. Pretty sure men can't have hysterectomies.
Because genital mutilation in men is the mutilation of the forskin that only males can have.
Every disease/disorder/syndrome/condition you mentioned proves my point exactly. All I had to do was Google all of these to see how rare or common they are. Actually, I google "How common is..." and almost each one said they these are rare conditions.
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