MeSH Browser

MeSH Supplementary: Focal cortical dysplasia of Taylor
Unique ID: C537067
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537067
Entry Term(s): Cortical Dysplasia of Taylor with Balloon Cells; Cortical dysplasia of Taylor; FCDT; Focal Cortical Dysplasia of Taylor, Type IIa; Focal Cortical Dysplasia of Taylor, Type IIb; Focal Cortical Dysplasia, Type II; Focal cortical dysplasia, type 2
Registry Numbers: 0
Previous Indexing: Malformations of Cortical Development (2010-2014)
Heading Mapped to: *Epilepsy; *Malformations of Cortical Development, Group I
Frequency: 199
Note: A cerebral developmental malformation that results in intractable EPILEPSY usually requiring surgery. FCDT is classified histologically into 2 subtypes: a type without balloon cells (Type IIA); and a type with balloon cells (Type IIB). Germline mutations in the TSC1 gene have been identified. OMIM: 607341
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Concept UI: M0531528
Registry Numbers: 0
Terms: Focal cortical dysplasia of Taylor Preferred Term
Term UI T741347
Date02/24/2009
LexicalTag NON
ThesaurusID; FCDT
Term UI T000882725
Date06/29/2015
LexicalTag NON
ThesaurusID OMIM (2013); Cortical dysplasia of Taylor
Term UI T741349
Date02/24/2009
LexicalTag NON
ThesaurusID; Focal cortical dysplasia, type 2
Term UI T741351
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Focal Cortical Dysplasia, Type II
Term UI T831199
Date10/12/2012
LexicalTag NON
ThesaurusID OMIM (2013)

Focal cortical dysplasia of Taylor MeSH Supplementary Concept Data 2025