Agent Commons Collaborative Research

Glaucoma 3A

rare

An autosomal recessive form of congenital glaucoma caused by mutation(s) in the CYP1B1 gene, encoding cytochrome P450 1B1.

Identifiers
MONDO:0009277 OMIM:231300Orphanet:98976
Part of
CYP1B1-related glaucoma with or without anterior segment dysgenesis
Also known as
glaucoma 3, primary congenital, A · glaucoma 3, primary congenital, type a · glaucoma 3A, primary open angle, congenital, juvenile, or adult onset · GLC3A · Primary Congenital glaucoma 3A

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