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Spastic Paraplegia 42, Autosomal Dominant
MeSH Supplementary Concept Data 2024
Details
Concepts
MeSH Supplementary
Spastic Paraplegia 42, Autosomal Dominant
Unique ID
C567262
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567262
Registry Number
0
Heading Mapped to
*Spastic Paraplegia, Hereditary
Frequency
1
Note
also known as SPG42
Date of Entry
2012/08/24
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Spastic Paraplegia 42, Autosomal Dominant
Preferred
Concept UI
M0567562
Registry Number
0
Terms
Spastic Paraplegia 42, Autosomal Dominant
Preferred Term
Term UI
T810065
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
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