Cone rod dystrophy
A rare genetic isolated inherited retinal disorder characterized by primary cone degeneration with significant secondary rod involvement with a variable fundus appearance. Typical presentation includes decreased visual acuity central scotoma photophobia color vision alteration followed by night blindness and loss of peripheral visual field.
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 December 2023
Newly diagnosed with
Cone rod dystrophy?
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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.