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Iridogoniodysgenesis, dominant type MeSH Supplementary Concept Data 2022


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 Preferred
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