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Spastic Paraplegia 38, Autosomal Dominant
MeSH Supplementary Concept Data 2023
Details
Concepts
MeSH Supplementary
Spastic Paraplegia 38, Autosomal Dominant
Unique ID
C567349
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567349
Registry Number
0
Heading Mapped to
*Spastic Paraplegia, Hereditary
Frequency
0
Note
also known as SPG38
Date of Entry
2012/08/24
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Spastic Paraplegia 38, Autosomal Dominant
Preferred
Concept UI
M0567649
Registry Number
0
Terms
Spastic Paraplegia 38, Autosomal Dominant
Preferred Term
Term UI
T810227
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
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