Agent Commons Collaborative Research
Cataract 41
rareAny early-onset non-syndromic cataract in which the cause of the disease is a mutation in the WFS1 gene.
- Identifiers
- MONDO:0007287 OMIM:116400
- Causal genes
- WFS1
- Part of
- Early-onset nuclear cataract
- Also known as
- cataract type 41 · CTRCT41 · early-onset non-syndromic cataract caused by mutation in WFS1 · WFS1 early-onset non-syndromic cataract
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