| Hereditary acrodermatitis enteropathica (disorder) | | Hereditary acrodermatitis enteropathica | | Brandt syndrome Hereditary acrodermatitis enterohepatica Danbolt-Close syndrome Danbolt-Closs syndrome Primary zinc malabsorption syndrome AE - Acrodermatitis enteropathica Acrodermatitis enteropathica Primary zinc malabsorption
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| | Id | 37702000 | | Status | Primitive |
| SNOMED CT to Orphanet simple map |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E83.2 | | Term | Stoornissen van zinkmetabolisme |
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| SNOMED CT to ICD-10 extended map | | Target | E83.2 | | Rule | TRUE | | Advice | ALWAYS E83.2 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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