MeSH Browser

MeSH Supplementary: Mainzer-Saldino Disease
Unique ID: C535463
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535463
Entry Term(s): Conorenal Syndrome; Mainzer-Saldino Syndrome; Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia; Saldino-Mainzer disease
Registry Number: 0
Heading Mapped to: *Cerebellar Ataxia; *Retinitis Pigmentosa
Frequency: 14
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Mainzer-Saldino Disease MeSH Supplementary Concept Data 2024