| Renal carnitine transport defect (disorder) | | Renal carnitine transport defect | | Carnitine uptake defect
Primary carnitine deficiency
Systemic carnitine deficiency
SLC22A5-gene related renal carnitine transport defect
Carnitine transporter deficiency
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| | Id | 21764004 | | Status | Primitive |
| SNOMED CT to Orphanet simple map |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E71.3 | | Term | Stoornissen van vetzuurmetabolisme |
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| SNOMED CT to ICD-10 extended map | | Target | E71.3 | | Rule | TRUE | | Advice | ALWAYS E71.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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