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Modifier, X-Linked, for Neurofunctional Defects MeSH Supplementary Concept Data 2025


MeSH Supplementary
Modifier, X-Linked, for Neurofunctional Defects
Unique ID
C564098
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C564098
Entry Term(s)
Tourette Syndrome, Modifier of
Registry Numbers
0
Heading Mapped to
*Tourette Syndrome
*Genetic Diseases, X-Linked
Frequency
0
Date of Entry
2012/11/05
Revision Date
1955/01/01
Modifier, X-Linked, for Neurofunctional Defects Preferred
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