| lissencefalie gelijktijdig met congenitale cerebellaire hypoplasie type F (aandoening) | | lissencefalie gelijktijdig met congenitale cerebellaire hypoplasie type F | | lissencefalie gelijktijdig met cerebellaire hypoplasie type F
| | Lissencephaly with cerebellar hypoplasia type F | | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F
| | A severe form of lissencephaly with cerebellar hypoplasia, characterized by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum. |
| | Id | 715822007 | | Status | Primitive |
| SNOMED CT to Orphanet simple map |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q04.3 | | Term | Overige onderontwikkeling van hersenen |
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| SNOMED CT to ICD-10 extended map | | Target | Q04.3 | | Rule | TRUE | | Advice | ALWAYS Q04.3 | 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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