Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A (disorder) | | Lissencephaly with cerebellar hypoplasia type A | | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A
| | A rare genetic lissencephaly with cerebellar hypoplasia subtype with characteristics of classical lissencephaly with thickened cortical gray matter (with either no discernable gradient, a predominantly posterior gradient, or a predominantly anterior gradient) associated with variable predominantly midline cerebellar hypoplasia. | | lissencefalie gelijktijdig met congenitale cerebellaire hypoplasie type A | | lissencefalie gelijktijdig met cerebellaire hypoplasie type A
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| Id | 785307003 | 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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