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Megalocornea MeSH Supplementary Concept Data 2022


MeSH Supplementary
Megalocornea
Unique ID
C562829
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C562829
Entry Term(s)
MGC1
MGCN
Registry Number
0
Heading Mapped to
*Eye Diseases, Hereditary
*Genetic Diseases, X-Linked
Frequency
70
Note
A hereditary X-linked eye disorder in which the corneal diameter is bilaterally enlarged (greater than 13 mm) without an increase in intraocular pressure. It is associated with mutations in the CHRDL1 gene. OMIM: 309300
Date of Entry
2012/11/05
Revision Date
2016/08/01
Megalocornea Preferred
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