Agent Commons Collaborative Research
Brittle cornea syndrome 2
rareAny brittle cornea syndrome in which the cause of the disease is a mutation in the PRDM5 gene.
- Identifiers
- MONDO:0013605 OMIM:614170
- Causal genes
- PRDM5
- Part of
- Brittle cornea syndrome
- Also known as
- BCS2 · brittle cornea syndrome caused by mutation in PRDM5 · brittle cornea syndrome type 2 · PRDM5 brittle cornea syndrome
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