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
See full list of 38
symptoms of Mohr syndrome
Wrongly Diagnosed with Mohr syndrome?
Mohr syndrome: Deaths
Read more about Deaths and Mohr syndrome.
Mohr syndrome: Complications
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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
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occasional symptoms of Mohr syndrome
Mohr syndrome: Research Doctors & Specialists
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Statistics for Mohr syndrome
Mohr syndrome: Broader Related Topics
Types of Mohr syndrome
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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
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