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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
Id785307003
StatusPrimitive
Associated morphologyHypoplasia
Finding siteCerebellar structure
OccurrenceCongenital
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ04.3
RuleTRUE
AdviceALWAYS Q04.3
CorrelationSNOMED CT source code to target map code correlation not specified