MeSH Browser

MeSH Supplementary: Hyperphenylalaninemia, BH4-Deficient, Due To Partial PTS Deficiency
Unique ID: C567493
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567493
Registry Numbers: 0
Heading Mapped to: *Phenylketonurias
Frequency: 0
Note: mutations in PTS
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Hyperphenylalaninemia, BH4-Deficient, Due To Partial PTS Deficiency MeSH Supplementary Concept Data 2025