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syndroom van ring chromosoom14 (aandoening)
syndroom van ring chromosoom14
ringchromosoom 14-syndroom
Ring chromosome 14 syndrome
Ring chromosome 14
Ring 14 syndrome
Disease with characteristics of intellectual deficit, retinal and skin pigmentation disorders, seizures, and dysmorphic features, including flat occiput, epicanthal folds, downward slanting eyes, flat nasal bridge, upturned nostrils, short neck and large low set ears.
Id702345009
StatusDefined
Associated morphologyringchromosoom
Finding sitechromosomenpaar 14
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
DHD Diagnosis thesaurus reference set
SNOMED CT to Orphanet simple map1440
SNOMED CT to ICD-10 extended map
TargetQ93.2
RuleTRUE
AdviceALWAYS Q93.2
CorrelationSNOMED CT source code to target map code correlation not specified