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Ermine phenotype

Ermine phenotype: Introduction

Ermine phenotype: A very rare syndrome characterized by pigmentation abnormalities as well as deafness. More detailed information about the symptoms, causes, and treatments of Ermine phenotype is available below.

Symptoms of Ermine phenotype

Home Diagnostic Testing

Home medical testing related to Ermine phenotype:

Wrongly Diagnosed with Ermine phenotype?

Ermine phenotype: Complications

Read more about complications of Ermine phenotype.

Causes of Ermine phenotype

Read more about causes of Ermine phenotype.

Misdiagnosis and Ermine phenotype

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Ermine phenotype: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Ermine phenotype: Animations

Statistics for Ermine phenotype

Ermine phenotype: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Ermine phenotype, or answer someone else's question, on our message boards:

Definitions of Ermine phenotype:

Ermine phenotype is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Ermine phenotype, or a subtype of Ermine phenotype, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Ermine phenotype Info

More information about Ermine phenotype

  1. Ermine phenotype: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications

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