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autosomaal dominante hereditaire arginine-vasopressinedeficiƫntie (aandoening)
autosomaal dominante hereditaire arginine-vasopressinedeficiƫntie
autosomaal dominante erfelijke centrale diabetes insipidus
Autosomal dominant hereditary vasopressin deficiency
Autosomal dominant hereditary AVP-D (arginine vasopressin deficiency)
Autosomal dominant hereditary arginine vasopressin deficiency
Id1296914004
StatusDefined
SNOMED CT to ICD-10 extended map
TargetE23.2
RuleTRUE
AdviceALWAYS E23.2
CorrelationSNOMED CT source code to target map code correlation not specified