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Spastic Paraplegia 39, Autosomal Recessive MeSH Supplementary Concept Data 2024


MeSH Supplementary
Spastic Paraplegia 39, Autosomal Recessive
Unique ID
C567433
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567433
Entry Term(s)
NTE-Related Motor Neuron Disorder
NTEMND
SPG39
Registry Number
0
Heading Mapped to
*Spastic Paraplegia, Hereditary
Frequency
1
Note
mutation in PNPLA6
Date of Entry
2012/11/05
Spastic Paraplegia 39, Autosomal Recessive Preferred
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