Hypertryptophanemia, Familial MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Hypertryptophanemia, Familial
Unique ID: C563467
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563467
Entry Term(s): Hypertryptophanemia
Registry Numbers: 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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