Disorder of sulfur-bearing amino acid metabolism	Metabolic renal disease	Specific renal tubule transport defect
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Familial methionine malabsorption (disorder)
	Familial methionine malabsorption
	Methionine malabsorption syndrome Beery-baby syndrome Oasthouse disease Oast-house disease Oast-house urine disease Smith-Strang disease
	familiaire methioninemalabsorptie
	familiaire malabsorptie van methionine

Id	45812003
Status	Primitive

Finding site

Kidney structure

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