Conradi-Hunermann syndrome: A rare genetic disorder characterized by growth deficiency, short limbs, large skin pores, sparse hair and other abnormalities. More detailed information about the symptoms, causes, and treatments of Conradi-Hunermann syndrome is available below.
See full list of 18 symptoms of Conradi-Hunermann syndrome
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See full list of 21 occasional symptoms of Conradi-Hunermann syndrome
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Types of Conradi-Hunermann syndrome
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Conradi-Hunermann syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Conradi-Hunermann syndrome, or a subtype of Conradi-Hunermann 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 Conradi-Hunermann syndrome as a "rare disease".
Source - Orphanet
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