Keratitis, hereditary MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Keratitis, hereditary
Unique ID: C537022
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537022
Entry Term(s): Dominantly inherited keratitis
Registry Numbers: 0
Heading Mapped to: Keratitis / congenital
Frequency: 3
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Keratitis, hereditary Preferred

page delivered in 0.006s