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Spastic Paraplegia 42, Autosomal Dominant MeSH Supplementary Concept Data 2022


MeSH Supplementary
Spastic Paraplegia 42, Autosomal Dominant
Unique ID
C567262
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567262
Entry Term(s)
Registry Number
0
Heading Mapped to
*Spastic Paraplegia, Hereditary
Frequency
1
Note
also known as SPG42
Date of Entry
2012/08/24
Spastic Paraplegia 42, Autosomal Dominant Preferred
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