MeSH Browser

MeSH Supplementary: Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial
Unique ID: C564890
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564890
Entry Term(s): Phosphoenolpyruvate carboxykinase 2 deficiency
Registry Numbers: 0
Heading Mapped to: *Carbohydrate Metabolism, Inborn Errors; Phosphoenolpyruvate Carboxykinase (ATP) / deficiency; *Mitochondrial Diseases
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 2022/11/02

Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial MeSH Supplementary Concept Data 2025