Chondrodystrophia calcificans congenita: A rare genetic disorder characterized by growth deficiency, short limbs, large skin pores, sparse hair and other abnormalities. More detailed information about the symptoms, causes, and treatments of Chondrodystrophia calcificans congenita is available below.
See full list of 18 symptoms of Chondrodystrophia calcificans congenita
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See full list of 21 occasional symptoms of Chondrodystrophia calcificans congenita
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Chondrodystrophia calcificans congenita as a "rare disease".
Source - Orphanet
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