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Mohr syndrome

Mohr syndrome: Introduction

Mohr syndrome: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger abnormalities. More detailed information about the symptoms, causes, and treatments of Mohr syndrome is available below.

Symptoms of Mohr syndrome

Wrongly Diagnosed with Mohr syndrome?

Mohr syndrome: Deaths

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Mohr syndrome: Complications

Review possible medical complications related to Mohr syndrome:

Causes of Mohr syndrome

Read more about causes of Mohr syndrome.

Disease Topics Related To Mohr syndrome

Research the causes of these diseases that are similar to, or related to, Mohr syndrome:

Less Common Symptoms of Mohr syndrome

Mohr syndrome: Research Doctors & Specialists

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Other doctor, physician and specialist research services:

Statistics for Mohr syndrome

Mohr syndrome: Broader Related Topics

User Interactive Forums

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Definitions of Mohr syndrome:

Mohr syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Mohr syndrome, or a subtype of Mohr 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 Mohr syndrome as a "rare disease".
Source - Orphanet

Related Mohr syndrome Info

Videos about Mohr syndrome

 

More information about Mohr syndrome

  1. Mohr syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Deaths
  7. Complications
 

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