| Autosomal dominant hereditary arginine vasopressin deficiency (disorder) | | 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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