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Use the form below to explore NORD's comprehensive rare disease database. Search for detailed information on rare diseases, including NORD's authoritative Rare Disease Reports and data from other reliable sources.
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brittle cornea syndrome 2

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Any brittle cornea syndrome in which the cause of the disease is a mutation in the PRDM5 gene.

Synonyms

  • BCS2
  • PRDM5 brittle cornea syndrome
  • brittle cornea syndrome 2
  • brittle cornea syndrome caused by mutation in PRDM5
  • brittle cornea syndrome type 2BCS2
  • PRDM5 brittle cornea syndrome
  • brittle cornea syndrome 2
  • brittle cornea syndrome caused by mutation in PRDM5
  • brittle cornea syndrome type 2
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