Glaucoma 1, Open Angle, P [Supplementary Concept]
A hereditary, autosomal dominant form of glaucoma that is characterized by cupping of the optic nerve head and visual field defects but no increase in intraocular pressure. It primarily affects younger patients and is associated with a 300 kb duplication in the q region of chromosome 12 (12q14) OMIM: 177700
Date introduced: November 5, 2012
MeSH Unique ID: C566748
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