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Cataract, Congenital, Cerulean Type, 3(CCA3)

MedGen UID:
324668
•Concept ID:
C1837023
•
Disease or Syndrome
Synonym: Cataract, Congenital Blue Dot Type, 3
 
OMIM®: 115700

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Clinical prediction guides

A novel locus for autosomal dominant congenital cerulean cataract maps to chromosome 12q.
Berry V, Ionides AC, Moore AT, Bhattacharya SS
Eur J Hum Genet 2011 Dec;19(12):1289-91. Epub 2011 Jul 6 doi: 10.1038/ejhg.2011.130. PMID: 21731060Free PMC Article

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