| xanthinurie type II met deficiëntie van molybdeencofactor in complementatiegroep C (aandoening) | | xanthinurie type II met deficiëntie van molybdeencofactor in complementatiegroep C | | xanthinurie door molybdeencofactordeficiëntie type C
| | Molybdenum cofactor deficiency complementation group C | | A subtype of molybdenum cofactor deficiency caused by GPHN gene mutation. |
| | Id | 1003387003 | | Status | Primitive |
| 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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