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sporadische foetale hersendisruptiesequentie (aandoening)
sporadische foetale hersendisruptiesequentie
Sporadic fetal brain disruption sequence
A rare non-syndromic central nervous system malformation disorder with characteristics of severe microcephaly, overlapping sutures, keel-like occipital bone prominence, scalp rugae with normal hair pattern and signs of neurological impairment. Brain imaging may show ventriculomegaly, cortical tissue deficit, and hydranencephaly.
Id763717004
StatusPrimitive
Has interpretationonder referentiebereik
Interpretshoofdomtrek
Associated morphologyverandering in groei
Finding sitestructuur van hoofd
Occurrencefoetale periode
Pathological processproces van pathologische ontwikkeling
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ02
TermMicrocefalie
SNOMED CT to Orphanet simple map1665
SNOMED CT to ICD-10 extended map
TargetQ02
RuleTRUE
AdviceALWAYS Q02 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified