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Anterior segment mesenchymal dysgenesis MeSH Supplementary Concept Data 2022


MeSH Supplementary
Anterior segment mesenchymal dysgenesis
Unique ID
C537775
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C537775
Entry Term(s)
Anterior segment ocular dysgenesis
Registry Number
0
Heading Mapped to
*Eye Abnormalities
Frequency
48
Note
A hereditary autosomal dominant eye abnormality characterized by anterior segment ocular dysgenesis, corneal opacity, cataracts, and normal to reduced visual acuity. Cornea and lens histology are abnormal. Mutations in the FOXE3 and PITX3 genes have been identified. OMIM: 107250
Date of Entry
2010/08/25
Revision Date
2015/08/17
Anterior segment mesenchymal dysgenesis Preferred
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