MeSH Browser

MeSH Supplementary: Facioscapulohumeral muscular dystrophy 1a
Unique ID: C536391
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536391
Entry Term(s): FSHD1A; FSHMD1A; Facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles; Facioscapulohumeral muscular dystrophy, infantile; Landouzy-dejerine muscular dystrophy; Muscular dystrophy, facioscapulohumeral, type 1a
Registry Number: 0
Heading Mapped to: *Muscular Dystrophy, Facioscapulohumeral
Frequency: 34
Note: PROM
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Facioscapulohumeral muscular dystrophy 1a MeSH Supplementary Concept Data 2023