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Spastic paraplegia 15, autosomal recessive MeSH Supplementary Concept Data 2022


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
Registry Number
0
Heading Mapped to
*Retinal Degeneration
*Spastic Paraplegia, Hereditary
Frequency
8
Date of Entry
2010/08/25
Revision Date
2012/11/05
Spastic paraplegia 15, autosomal recessive Preferred
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