autosomaal recessieve hereditaire arginine-vasopressinedeficiƫntie (aandoening) | | autosomaal recessieve hereditaire arginine-vasopressinedeficiƫntie | | autosomaal recessieve erfelijke centrale diabetes insipidus
| | Autosomal recessive hereditary arginine vasopressin deficiency | | Autosomal recessive hereditary vasopressin deficiency Autosomal recessive hereditary AVP-D (arginine vasopressin deficiency)
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| Id | 1296915003 | 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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