Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F (disorder) | | Lissencephaly with cerebellar hypoplasia type F | | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F
| | A severe form of lissencephaly with cerebellar hypoplasia with main features microcephaly of at least 3 standard deviations and a thick cortex associated with complete absence of the corpus callosum. | | lissencefalie gelijktijdig met congenitale cerebellaire hypoplasie type F | | lissencefalie gelijktijdig met cerebellaire hypoplasie type F
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| Id | 715822007 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | Q04.3 | Rule | TRUE | Advice | ALWAYS Q04.3 | Correlation | SNOMED CT source code to target map code correlation not specified |
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