|
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 with main features microcephaly of at least 3 standard deviations and a thick cortex associated with complete absence of the corpus callosum.
Id715822007
StatusPrimitive
Associated morphologyhypoplasie
Finding sitestructuur van cerebellum
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ04.3
TermOverige onderontwikkeling van hersenen
SNOMED CT to Orphanet simple map100016
SNOMED CT to ICD-10 extended map
TargetQ04.3
RuleTRUE
AdviceALWAYS Q04.3
CorrelationSNOMED CT source code to target map code correlation not specified