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

cataract 46 juvenile-onset | RareConnect | RareConnect.io

/early-onset non-syndromic cataract

/cataract 46 juvenile-onset

cataract 46 juvenile-onset

Rare Disease

MONDO:0008925

Also Known As

CTRCT46LEMD2 early-onset non-syndromic cataractearly-onset non-syndromic cataract caused by mutation in LEMD2juvenilae cataract Hutterite typecataract 46, juvenile-onsetcataract Hutterite typecataract, congenital or juvenilecataract, juvenile, Hutterite type

Definition

Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the LEMD2 gene.

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:212500 ↗

Orphanet

Orphanet:98987 ↗

GARD

Related Diseases

cataract 32 multiple types

MONDO:0007278

cataract 8 multiple types

MONDO:0007280

cataract 42

MONDO:0007283

cataract 20 multiple types

MONDO:0007284

cataract 6 multiple types

MONDO:0007288

cataract 13 with adult I phenotype

MONDO:0007289

← Back to All Diseases