Frontometaphyseal dysplasia: A rare genetic disorder characterized by craniofacial abnormalities, skeletal abnormalities, hearing problems and wasting of arm and leg muscles. More detailed information about the symptoms, causes, and treatments of Frontometaphyseal dysplasia is available below.
See full list of 40 symptoms of Frontometaphyseal dysplasia
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See full list of 6 occasional symptoms of Frontometaphyseal dysplasia
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Types of Frontometaphyseal dysplasia
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Frontometaphyseal dysplasia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Frontometaphyseal dysplasia, or a subtype of Frontometaphyseal dysplasia,
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 Frontometaphyseal dysplasia as a "rare disease".
Source - Orphanet
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