4-Hydroxyphenylpyruvate dioxygenase deficiency	4-Hydroxyphenylpyruvate dioxygenase deficiency	Autosomal dominant hereditary disorder	Autosomal dominant hereditary disorder	Disorder of sulfur-bearing amino acid metabolism	Disorder of sulfur-bearing amino acid metabolism	Hereditary metabolic disease
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Hawkinsinuria (disorder)
	Hawkinsinuria
	hawkinsinurie

Id	414380008
Status	Primitive

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E72.1
Rule	TRUE
Advice	ALWAYS E72.1
Correlation	SNOMED CT source code to target map code correlation not specified