MeSH Browser

MeSH Supplementary: Neuromuscular Disease, Congenital, With Uniform Type 1 Fiber
Unique ID: C567162
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567162
Entry Term(s): CNMDU1
Registry Numbers: 0
Heading Mapped to: *Myopathy, Central Core
Frequency: 0
Note: PROM
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Neuromuscular Disease, Congenital, With Uniform Type 1 Fiber MeSH Supplementary Concept Data 2025