Autosomal recessive hereditary disorder
Deficiency of steroid 21-monooxygenase
Hereditary disorder of endocrine system
Inborn error of metabolism
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Moderate steroid 21-hydroxylase deficiency (disorder)
Moderate steroid 21-hydroxylase deficiency
matige steroïd-21-hydroxylasedeficiëntie
matige deficiëntie van steroïd-21-hydroxylase
Id60045007
StatusPrimitive
Finding siteAdrenal cortex structure
OccurrenceCongenital
ICD-10 complex map reference set
TargetE25.0
RuleTRUE
AdviceALWAYS E25.0
CorrelationSNOMED CT source code to target map code correlation not specified