MeSH Browser

MeSH Supplementary: Kocher-Debre-Semelaigne syndrome
Unique ID: C537211
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537211
Entry Term(s): Kocher Debre Semelaigne disease
Registry Numbers: 0
Heading Mapped to: *Congenital Hypothyroidism; *Hypertrophy; *Muscular Diseases; Muscle, Skeletal / pathology
Frequency: 17
Note: Association of muscular pseudohypertrophy and hypothyroidism in children
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Kocher-Debre-Semelaigne syndrome MeSH Supplementary Concept Data 2025