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Hypotrichosis simplex

Hypotrichosis simplex: Introduction

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.

Symptoms of Hypotrichosis simplex

Wrongly Diagnosed with Hypotrichosis simplex?

Hypotrichosis simplex: Complications

Read more about complications of Hypotrichosis simplex.

Causes of Hypotrichosis simplex

Read more about causes of Hypotrichosis simplex.

Misdiagnosis and Hypotrichosis simplex

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Hypotrichosis simplex: Animations

 

Statistics for Hypotrichosis simplex

Hypotrichosis simplex: Broader Related Topics

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Definitions of Hypotrichosis simplex:

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

Related Hypotrichosis simplex Info

More information about Hypotrichosis simplex

  1. Hypotrichosis simplex: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications
 

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