MeSH Browser

MeSH Supplementary: Spastic paraplegia 3, autosomal dominant
Unique ID: C536864
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536864
Entry Term(s): Familial spastic paraplegia, autosomal dominant, 1; Fsp1 Familial spastic paraplegia 1; SPG3A Spastic paraplegia 3a; Spastic Paraplegia 3; Spastic Paraplegia 3a; Spastic Paraplegia Type 3a; Spg3a; Strumpell disease
Registry Number: 0
Heading Mapped to: *Spastic Paraplegia, Hereditary
Frequency: 28
Note: Hereditary autosomal dominant spastic paraplegia that is associated with mutations in the ATL1 gene. OMIM: 182600
Date of Entry: 2010/08/25
Revision Date: 2019/06/20

Concept UI: M0531325
Registry Number: 0
Terms: Spastic paraplegia 3, autosomal dominant Preferred Term
Term UI T740691
Date02/24/2009
LexicalTag NON
ThesaurusID; Spastic Paraplegia Type 3a
Term UI T000880803
Date05/29/2015
LexicalTag NON
ThesaurusID GHR (2014); Spastic Paraplegia 3
Term UI T000880804
Date05/29/2015
LexicalTag NON
ThesaurusID GHR (2014); SPG3A Spastic paraplegia 3a
Term UI T000961322
Date06/19/2019
LexicalTag NON
ThesaurusID NLM (2019); Spg3a
Term UI T000880806
Date05/29/2015
LexicalTag NON
ThesaurusID GHR (2014); Strumpell disease
Term UI T740694
Date02/24/2009
LexicalTag NON
ThesaurusID; Familial spastic paraplegia, autosomal dominant, 1
Term UI T740695
Date02/24/2009
LexicalTag NON
ThesaurusID; Fsp1 Familial spastic paraplegia 1
Term UI T000961480
Date06/20/2019
LexicalTag NON
ThesaurusID NLM (2019); Spastic Paraplegia 3a
Term UI T000880805
Date05/29/2015
LexicalTag NON
ThesaurusID GHR (2014)

Spastic paraplegia 3, autosomal dominant MeSH Supplementary Concept Data 2024