MeSH Browser

MeSH Supplementary: Spastic paraplegia 15, autosomal recessive
Unique ID: C536642
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536642
Entry Term(s): Kjellin syndrome; Recessive spastic paraplegia with retinal degeneration; Spastic paraplegia and retinal degeneration
Heading Mapped to: *Retinal Degeneration; *Spastic Paraplegia, Hereditary
Frequency: 9
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Spastic paraplegia 15, autosomal recessive MeSH Supplementary Concept Data 2024