Jansen type metaphyseal chondrodysplasia: A rare genetic disorder characterized by extremely short stature, unusual face and skeletal and joint abnormalities. More detailed information about the symptoms, causes, and treatments of Jansen type metaphyseal chondrodysplasia is available below.
See full list of 22 symptoms of Jansen type metaphyseal chondrodysplasia
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Review possible medical complications related to Jansen type metaphyseal chondrodysplasia:
Research the causes of these diseases that are similar to, or related to, Jansen type metaphyseal chondrodysplasia:
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Jansen 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 Jansen type metaphyseal chondrodysplasia, or a subtype of Jansen 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 Jansen type metaphyseal chondrodysplasia as a "rare disease".
Source - Orphanet
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