| syndroom van koortsgerelateerd acuut infantiel leverfalen (aandoening) | | syndroom van koortsgerelateerd acuut infantiel leverfalen | | recidiverend acuut leverfalen door koorts bij zuigeling
koortsgerelateerd acuut infantiel leverfalen
| | Fever-associated acute infantile liver failure syndrome | | A rare genetic parenchymatous liver disease with characteristics of infantile or early childhood onset of recurrent episodes of acute liver failure precipitated by a febrile illness. During the life-threatening episodes, patients present with vomiting, lethargy, jaundice as well as elevated levels of liver enzymes and coagulopathy. There is usually complete recovery between the episodes with conservative treatment. |
| | Id | 1208726006 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 464724 |
| SNOMED CT to ICD-10 extended map | | Target | K72.0 | | Rule | TRUE | | Advice | ALWAYS K72.0 | 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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