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Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations MeSH Supplementary Concept Data 2022


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 Number
0
Heading Mapped to
*Mental Retardation, X-Linked
Frequency
3
Date of Entry
2012/11/05
Revision Date
2014/06/02
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Preferred
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