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Spastic Paraplegia 44, Autosomal Recessive
MeSH Supplementary Concept Data 2024
Details
Concepts
MeSH Supplementary
Spastic Paraplegia 44, Autosomal Recessive
Unique ID
C567707
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567707
Heading Mapped to
*Spastic Paraplegia, Hereditary
Frequency
0
Note
also known as SPG44; associated with mutations of GJC2 gene which encodes gap junction protein, gamma-2
Date of Entry
2012/08/24
Revision Date
1955/01/01
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Spastic Paraplegia 44, Autosomal Recessive
Preferred
Concept UI
M0568007
Terms
Spastic Paraplegia 44, Autosomal Recessive
Preferred Term
Term UI
T810921
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
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