MeSH Browser

MeSH Supplementary: CDKL5 deficiency disorder
Unique ID: C564064
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564064
Entry Term(s): CDKL5 Disorder; Epileptic Encephalopathy, Early Infantile, 2; Infantile Spasm Syndrome, X-Linked 2; Rett Syndrome, Atypical, Cdkl5-Related; Rett Syndrome, Variant, With Infantile Spasms
Registry Numbers: 0
Heading Mapped to: *Spasms, Infantile; *Epileptic Syndromes
Frequency: 173
Date of Entry: 2012/11/05
Revision Date: 2019/04/09

CDKL5 deficiency disorder MeSH Supplementary Concept Data 2025