Cerebelloparenchymal autosomal recessive disorder 3: A rare, recessively inherited disorder characterized mainly by albinism, incoordination, low muscle tone and eye problems. More detailed information about the symptoms, causes, and treatments of Cerebelloparenchymal autosomal recessive disorder 3 is available below.
See full list of 14 symptoms of Cerebelloparenchymal autosomal recessive disorder 3
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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 Cerebelloparenchymal autosomal recessive disorder 3 as a "rare disease".
Source - Orphanet
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