Blue Cone Monochromacy > Forms and Contacts

Forms and Contacts

This BCM Registry® is an online Patient Registry dedicated to a rare genetic retinal disease, Blue Cone Monochromacy. The Registry was created by BCM Families Foundation, a 501(c)(3) non-profit patient-led organization with the mission to cure BCM.

The BCM Patient Registry received funds from Otto per Mille della Chiesa Valdese.

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2019-2020-2021 Results have been reported in the BCMRegistry-Poster-2022-Final

2019-2020 Results have been reported in the BCMRegistry-Poster-Final

How to draw your family pedigree: Pedigree-Explanation

BCM Registry Consent Form

BCM Registry Assent Form

Terms & Conditions

Privacy Notice to Patients

BCM Registry Data Protection Impact Assessment (DPIA)