Toggle navigation
Search
Tree View
MeSH on Demand
MeSH 2025
About
Suggestions
Contact Us
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations
MeSH Supplementary Concept Data 2024
Details
Concepts
MeSH Supplementary
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations
Unique ID
C566878
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566878
Entry Term(s)
Mecp2-Related Severe Neonatal Encephalopathy
Registry Numbers
0
Heading Mapped to
*Mental Retardation, X-Linked
Frequency
3
Date of Entry
2012/11/05
Revision Date
2014/06/02
Expand All
Collapse All
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations
Preferred
Concept UI
M0567178
Registry Numbers
0
Terms
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations
Preferred Term
Term UI
T809323
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
Mecp2-Related Severe Neonatal Encephalopathy
Term UI
T841977
Date
04/18/2013
LexicalTag
NON
ThesaurusID
GHR (2014)
page delivered in 0.004s