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
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| Id | 1296914004 | Status | Defined |
SNOMED CT to ICD-10 extended map | Target | E23.2 | Rule | TRUE | Advice | ALWAYS E23.2 | Correlation | SNOMED CT source code to target map code correlation not specified |
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