Autosomal recessive hereditary disorder
Disorder of sulfur-bearing amino acid metabolism
Enzymopathy
Inborn error of metabolism
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Sulfite oxidase deficiency syndrome (disorder)
Sulfite oxidase deficiency syndrome
Sulfocysteinuria
sulfietoxidasedeficiëntiesyndroom
syndroom van deficiëntie van sulfietoxidase
Id40873003
StatusPrimitive
OccurrenceCongenital
ICD-10 complex map reference set
TargetE72.1
RuleTRUE
AdviceALWAYS E72.1
CorrelationSNOMED CT source code to target map code correlation not specified