MeSH Browser

MeSH Supplementary: Megalocornea
Unique ID: C562829
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562829
Entry Term(s): MGC1; MGCN
Registry Numbers: 0
Heading Mapped to: *Eye Diseases, Hereditary; *Genetic Diseases, X-Linked
Frequency: 78
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 MeSH Supplementary Concept Data 2025