Iridogoniodysgenesis, dominant type [Supplementary Concept]

Date introduced: August 25, 2010

MeSH Unique ID: C535536

Heading Mapped to:

• Anterior Chamber/abnormalities
• Eye Abnormalities
• Glaucoma
• Iris Diseases
• Tooth Abnormalities

Entry Terms:

• Iris hypoplasia with early onset glaucoma, autosomal dominant
• Iridogoniodysgenesis type 2
• Iridogoniodysgenesis syndrome
• Iridogoniodysgenesis, Type 2
• Iris Hypoplasia With Early-Onset Glaucoma, Autosomal Dominant