Coloboma chorioretinal cerebellar vermis aplasia: A very rare syndrome characterized by an eye anomaly (gap in eye structures such as choroids and retina) and abnormal development of the midline structure of the brain (cerebellar vermis aplasia). More detailed information about the symptoms, causes, and treatments of Coloboma chorioretinal cerebellar vermis aplasia is available below.
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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 Coloboma chorioretinal cerebellar vermis aplasia as a "rare disease".
Source - Orphanet
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