MeSH Browser

MeSH Supplementary: Cortical Dysplasia-Focal Epilepsy Syndrome
Unique ID: C567657
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567657
Entry Term(s): PTHSL1; Pitt-Hopkins-Like Syndrome 1
Registry Number: 0
Heading Mapped to: *Epilepsies, Partial; *Craniofacial Abnormalities; *Malformations of Cortical Development
Frequency: 18
Date of Entry: 2012/11/05
Revision Date: 2019/04/01

Cortical Dysplasia-Focal Epilepsy Syndrome MeSH Supplementary Concept Data 2024