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Glaucoma 1, Open Angle, P MeSH Supplementary Concept Data 2023


MeSH Supplementary
Glaucoma 1, Open Angle, P
Unique ID
C566748
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566748
Entry Term(s)
Pseudoglaucoma
Registry Number
0
Heading Mapped to
*Eye Diseases, Hereditary
Frequency
16
Note
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 of Entry
2012/11/05
Revision Date
2016/09/29
Glaucoma 1, Open Angle, P Preferred
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