MeSH Browser

MeSH Supplementary: Muscular dystrophy, congenital, infantile with cataract and hypogonadism
Unique ID: C537385
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537385
Entry Term(s): Familial congenital muscular dystrophy with gonadal dysgenesis; Muscular Dystrophy, Congenital, with Infantile Cataract and Hypogonadism
Registry Numbers: 0
Heading Mapped to: *Cataract; *Hypogonadism; Muscular Dystrophies / congenital
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Muscular dystrophy, congenital, infantile with cataract and hypogonadism MeSH Supplementary Concept Data 2025