MeSH Browser

MeSH Supplementary: Iridogoniodysgenesis, dominant type
Unique ID: C535536
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535536
Entry Term(s): Iridogoniodysgenesis syndrome; Iridogoniodysgenesis type 2; Iridogoniodysgenesis, Type 2; Iris Hypoplasia With Early-Onset Glaucoma, Autosomal Dominant; Iris hypoplasia with early onset glaucoma, autosomal dominant
Registry Number: 0
Heading Mapped to: Anterior Chamber / *abnormalities; *Eye Abnormalities; *Glaucoma; *Iris Diseases; *Tooth Abnormalities
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Iridogoniodysgenesis, dominant type MeSH Supplementary Concept Data 2024