Familial XX true hermaphroditism (medical condition): A very rare genetic disorder where a baby is born having both male and female internal sex organs.
See also:
Hermaphroditism:
»Introduction: Hermaphroditism
»Symptoms of Hermaphroditism
These medical condition or symptom topics may be relevant to medical information for Familial XX true hermaphroditism:
Familial XX true hermaphroditism is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Familial XX true hermaphroditism, or a subtype of Familial XX true hermaphroditism,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Familial XX true hermaphroditism: Another name for Hermaphroditism (or close medical condition association).
»Introduction: Hermaphroditism
»Symptoms of Hermaphroditism
Some of the symptoms of Familial XX true hermaphroditism incude:
See full list of 6 symptoms of Familial XX true hermaphroditism (Hermaphroditism)
These medical disease topics may be related to Familial XX true hermaphroditism:
Source - NIH
Search to find out more about Familial XX true hermaphroditism:
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