Autosomal recessive hereditary disorder	Autosomal recessive hereditary disorder	Disorder of sulfur-bearing amino acid metabolism	Disorder of sulfur-bearing amino acid metabolism	Hereditary metabolic disease	Vitamin disease	Vitamin disease
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Transcobalamin II deficiency (disorder)
	Transcobalamin II deficiency
	TCN2 - Transcobalamin II deficiency
	transcobalamine-2-deficiëntie

Id	237934001
Status	Primitive

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	D51.2
Rule	TRUE
Advice	ALWAYS D51.2
Correlation	SNOMED CT source code to target map code correlation not specified