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Iridogoniodysgenesis type1 MeSH Supplementary Concept Data 2022


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 Number
0
Heading Mapped to
*Eye Abnormalities
*Glaucoma
*Iris Diseases
Frequency
1
Date of Entry
2010/08/25
Revision Date
2012/11/05
Iridogoniodysgenesis type1 Preferred
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