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Hypertryptophanemia, Familial MeSH Supplementary Concept Data 2024


MeSH Supplementary
Hypertryptophanemia, Familial
Unique ID
C563467
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C563467
Entry Term(s)
Hypertryptophanemia
Registry Number
0
Heading Mapped to
*Amino Acid Metabolism, Inborn Errors
Frequency
9
Date of Entry
2012/11/05
Revision Date
2018/09/24
Hypertryptophanemia, Familial Preferred
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