Congenital cataract microcornea with corneal opacity
Synonyms: CCMCO
A rare genetic eye disease characterized by congenital cataract microcornea and corneal opacity resulting in severe visual impairment or blindness. Depending on the genetic background other developmental ocular defects may also be present.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
Congenital cataract microcornea with corneal opacity?
Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.
Advocacy Organizations
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.