Term Name: | pyridoxamine 5'-phosphate oxidase deficiency |
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Synonyms: | PNPO deficiency, PNPO-related neonatal epileptic encephalopathy, pyridoxal 5'-phosphate-dependent epilepsy, pyridoxal phosphate-dependent seizures, pyridoxal phosphate-responsive seizures, pyridoxamine 5'-oxidase deficiency, pyridoxamine 5-prime-phosphate oxidase deficiency |
Definition: | A vitamin metabolic disorder characterized by vitamin B6 deficienc resulting in neonatal-onset of severe seizures that can be controlled with pyridoxal 5'-phosphate treatment that has_material_basis_in homozygous or compound heterozygous mutation in PNPO on 17q21.32. |
Ontology: | Human Disease [DOID:0111329] ( DOID:0111329 ) |