Hypotrichosis simplex: Abnormally sparse hair caused by a genetic anomaly. More detailed information about the symptoms, causes, and treatments of Hypotrichosis simplex is available below.
Read more about complications of Hypotrichosis simplex.
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Hypotrichosis simplex is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Hypotrichosis simplex, or a subtype of Hypotrichosis simplex,
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 Hypotrichosis simplex as a "rare disease".
Source - Orphanet
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