MeSH Browser

MeSH Supplementary: Bassoe syndrome
Unique ID: C537661
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537661
Registry Numbers: 0
Heading Mapped to: Cataract / congenital; *Hypogonadism; *Muscular Dystrophies
Frequency: 0
Note: Benign muscular dystrophy with hypergonadotrophic hypogonadism and congenital cataract
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Bassoe syndrome MeSH Supplementary Concept Data 2025