MeSH Browser

MeSH Supplementary: Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency
Unique ID: C566449
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566449
Entry Term(s): Epileptic Encephalopathy, Neonatal, PNPO-Related; PNPO Deficiency; PNPO-Related Neonatal Epileptic Encephalopathy; Pyridoxal 5'-Phosphate-Dependent Epilepsy; Pyridoxine-5'-Phosphate Oxidase Deficiency; Seizures, Pyridoxine-Resistant, PLP-Sensitive
Registry Number: 0
Heading Mapped to: *Brain Diseases, Metabolic; Pyridoxaminephosphate Oxidase / *deficiency; *Seizures; *Hypoxia-Ischemia, Brain
Frequency: 23
Date of Entry: 2012/11/05
Revision Date: 2013/10/24

Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency MeSH Supplementary Concept Data 2024