MeSH Browser

MeSH Supplementary: Exudative vitreoretinopathy 1
Unique ID: C536382
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536382
Entry Term(s): Criswick-Schepens syndrome; Exudative vitreoretinopathy, familial, autosomal dominant; FEVR, Autosomal Dominant
Registry Number: 0
Previous Indexing: Osteoporosis(2013-2019); Vitreoretinopathy, Proliferative(2013-2019)
Heading Mapped to: *Familial Exudative Vitreoretinopathies
Frequency: 13
Date of Entry: 2010/08/25
Revision Date: 2019/04/08

Exudative vitreoretinopathy 1 MeSH Supplementary Concept Data 2024