Skip to main content

RareConnect.ioRare Intelligence

Explore Data Discover Patient Groups News Partner

Sign In Sign Up

Explore Data Patient Groups News Partner

RareConnect.ioRare Intelligence

Combining the speed of AI with the wisdom of the community to build the world's most accurate disease registry.

Explore

Disease Directory
Patient Groups
News
FAQ
MONDO Ontology ↗

Get Involved

Partner with Us
Register Your PAG
Community
Pricing

Legal

Privacy Policy
Terms of Service
Accessibility
Contact Us

© 2025 RareConnect.io. Powered by MONDO Ontology

retinal cone dystrophy 3A | RareConnect | RareConnect.io

/hereditary neurological disease

/retinal cone dystrophy 3A

retinal cone dystrophy 3A

Rare Disease

MONDO:0012398

Also Known As

retinal cone dystrophy 3retinal cone dystrophy 3Aretinal cone dystrophy type 3ARCD3Aachromatopsia 6cone dystrophy with night blindness and supernormal Rod responses, Pde6H-relatedcone dystrophy with night blindness and supernormal rod responses PDE6H-related

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:610024 ↗

GARD

Related Diseases

leukoencephalopathy, megalencephalic

MONDO:0000137

epilepsy, familial adult myoclonic

MONDO:0000160

encephalopathy, acute, infection-induced

MONDO:0000166

GLUT1 deficiency syndrome

MONDO:0000188

paraganglioma

MONDO:0000448

familial hemiplegic migraine

MONDO:0000700

← Back to All Diseases