MeSH Browser

MeSH Supplementary: Iridogoniodysgenesis type1
Unique ID: C535535
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535535
Entry Term(s): Iridogoniodysgenesis anomaly, Autosomal dominant; Iridogoniodysgenesis, Type 1
Registry Numbers: 0
Heading Mapped to: *Eye Abnormalities; *Glaucoma; *Iris Diseases
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Iridogoniodysgenesis type1 MeSH Supplementary Concept Data 2025