Autosomal recessive hereditary disorder	Autosomal recessive hereditary disorder	Congenital immunodeficiency disease	Congenital immunodeficiency disease	Disorder of purine metabolism	Disorder of purine metabolism	Enzymopathy	Enzymopathy	Hereditary metabolic disease
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Purine-nucleoside phosphorylase deficiency (disorder)
	Purine-nucleoside phosphorylase deficiency
	NP deficiency PNP - Purine nucleoside phosphorylase deficiency PNP deficiency Deficiency of inosine phosphorylase Deficiency of purine-nucleoside phosphorylase Purine nucleoside phosphorylase deficiency Nucleoside phosphorylase deficiency NP - Nucleoside phosphorylase deficiency
	deficiëntie van purinenucleosidefosforylase
	PNP-deficiëntie

Id	60743005
Status	Primitive

Occurrence

Occurrence

Pathological process

Abnormal immune process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	D81.5
Rule	TRUE
Advice	ALWAYS D81.5
Correlation	SNOMED CT source code to target map code correlation not specified