| cobalamin F disease (aandoening) | | cobalamin F disease | | cbl F
| | Inherited methylmalonic acidemia AND homocystinuria | | Cobalamin locus F variant
CblF - Cobalamin locus F variant
CblF methylmalonic acidemia and homocystinuria
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| | Id | 80887004 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E88.8 | | Term | Overige gespecificeerde stofwisselingsstoornissen |
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| SNOMED CT to Orphanet simple map | 26 |
| SNOMED CT to ICD-10 extended map | | Target | E72.1 | | Rule | TRUE | | Advice | ALWAYS E72.1 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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