Autosomal recessive hereditary disorder	Congenital neurological disorder	Disorder of neurometabolic regulation	Epilepsy	Hereditary disorder of endocrine system	Inherited metabolic disorder of nervous system
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Pyridoxine-dependent epilepsy (disorder)
	Pyridoxine-dependent epilepsy
	Antiquitin deficiency Vitamin B6-dependent seizures
	pyridoxineafhankelijke epilepsie
	vitamine B6-afhankelijke epilepsie

Id	734434007
Status	Primitive

Finding site

Finding site	Structure of endocrine system
Occurrence	Congenital

Finding site	Structure of central nervous system
Occurrence	Congenital

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G40.8
Rule	TRUE
Advice	ALWAYS G40.8
Correlation	SNOMED CT source code to target map code correlation not specified