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Dictionary » Familial true hermaphroditism
 

Familial true hermaphroditism

Introduction: Familial true hermaphroditism

Description of Familial true hermaphroditism

Familial true hermaphroditism (medical condition): A very rare genetic disorder where a baby is born having both male...more »

See also:

Hermaphroditism:
  »Introduction: Hermaphroditism
  »Symptoms of Hermaphroditism

Familial true hermaphroditism: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial true hermaphroditism:

Familial true hermaphroditism: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Familial 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 true hermaphroditism, or a subtype of Familial true hermaphroditism, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Familial true hermaphroditism as a Disease

Familial true hermaphroditism: Another name for Hermaphroditism (or close medical condition association).
  »Introduction: Hermaphroditism
  »Symptoms of Hermaphroditism

Familial true hermaphroditism: Related Diseases

Familial true hermaphroditism: Familial true hermaphroditism is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Familial true hermaphroditism (Hermaphroditism)

Some of the symptoms of Familial true hermaphroditism incude:

Familial true hermaphroditism: Related Disease Topics

These medical disease topics may be related to Familial true hermaphroditism:

  • androgyny
  • gonochorism
  • gyandromorph
  • morphodite
  • supernumerary body part

Terms associated with Familial true hermaphroditism:

Terms Similar to Familial true hermaphroditism:

Source - NIH

Interesting Medical Articles:

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