Theodor-Hertz-Goodman syndrome: A very rare syndrome characterized mainly by short stature, fused finger bones and extra testes. More detailed information about the symptoms, causes, and treatments of Theodor-Hertz-Goodman syndrome is available below.
See full list of 9 symptoms of Theodor-Hertz-Goodman syndrome
Read more about causes of Theodor-Hertz-Goodman syndrome
Read more about causes of Theodor-Hertz-Goodman syndrome.
More information about causes of Theodor-Hertz-Goodman syndrome:
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Theodor-Hertz-Goodman syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Theodor-Hertz-Goodman syndrome, or a subtype of Theodor-Hertz-Goodman syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Theodor-Hertz-Goodman syndrome as a "rare disease".
Source - Orphanet
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