Dimethylglycine Dehydrogenase Deficiency MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Dimethylglycine Dehydrogenase Deficiency
Unique ID: C565278
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565278
Entry Term(s): DMGDH Deficiency; DMGDHD
Registry Number: 0
Heading Mapped to: *Amino Acid Metabolism, Inborn Errors
Frequency: 1
Note: mutation in DMGDH
Date of Entry: 2012/11/05

Dimethylglycine Dehydrogenase Deficiency Preferred

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