MeSH Browser

MeSH Supplementary: Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant
Unique ID: C563392
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563392
Entry Term(s): ADRESD; RESDAD
Registry Numbers: 0
Heading Mapped to: *Apraxias; *Intellectual Disability; *Epilepsy, Rolandic
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant MeSH Supplementary Concept Data 2025