McKusick type metaphyseal chondrodysplasia: A rare genetic disorder characterized by short stature, skeletal abnormalities and fine, fragile hair. More detailed information about the symptoms, causes, and treatments of McKusick type metaphyseal chondrodysplasia is available below.
See full list of 46 symptoms of McKusick type metaphyseal chondrodysplasia
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See full list of 7 occasional symptoms of McKusick type metaphyseal chondrodysplasia
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McKusick type metaphyseal chondrodysplasia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that McKusick type metaphyseal chondrodysplasia, or a subtype of McKusick type metaphyseal chondrodysplasia,
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 McKusick type metaphyseal chondrodysplasia as a "rare disease".
Source - Orphanet
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