MeSH Browser

MeSH Supplementary: Pontocerebellar Hypoplasia Type 2B
Unique ID: C567325
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567325
Registry Numbers: 0
Heading Mapped to: *Cerebellar Diseases; Cerebellum / abnormalities; Pons / abnormalities
Frequency: 0
Note: aka PCH2B; mutations in TSEN2
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Pontocerebellar Hypoplasia Type 2B MeSH Supplementary Concept Data 2025