MeSH Browser

MeSH Supplementary: Nephrotic syndrome ocular anomalies
Unique ID: C536403
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536403
Entry Term(s): Familial infantile nephrotic syndrome with ocular abnormalities; Glastre Cochat Bouvier syndrome
Registry Number: 0
Heading Mapped to: *Eye Abnormalities; Nephrotic Syndrome / *congenital
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Nephrotic syndrome ocular anomalies MeSH Supplementary Concept Data 2024