MeSH Browser

MeSH Supplementary: Sclerocornea
Unique ID: C565209
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565209
Registry Number: 0
Heading Mapped to: Cornea / *abnormalities; *Corneal Diseases
Frequency: 35
Note: A hereditary abnormality characterized by scleralization or opacity of the peripheral or entire cornea. OMIM: 181700
Date of Entry: 2012/11/05
Revision Date: 2016/09/29

Sclerocornea MeSH Supplementary Concept Data 2024