MeSH Browser

MeSH Supplementary: Pontocerebellar Hypoplasia Type 3
Unique ID: C548072
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C548072
Entry Term(s): Cerebellar Atrophy With Progressive Microcephaly; Pch With Optic Atrophy
Registry Number: 0
Heading Mapped to: *Olivopontocerebellar Atrophies
Frequency: 9
Note: Pch3 not included
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Pontocerebellar Hypoplasia Type 3 MeSH Supplementary Concept Data 2024