congenitaal syndroom van Horner-pupil (aandoening)
congenitaal syndroom van Horner-pupil
congenitaal syndroom van ipsilaterale myose en ptose
congenitale Horner-pupil
Congenital Horner syndrome
Congenital Claude Bernard Horner syndrome
A rare neurological disorder with characteristics of relative pupillary miosis and blepharoptosis, evident at birth, caused by interruption of the oculosympathetic innervation at any point along the neural pathway from the hypothalamus to the orbit. Often additional symptoms, such as enophthalmos, facial anhidrosis, iris heterochromia, conjunctival congestion, transient hypotonia and/or pupillary dilation lag, may be present. Association with birth trauma, neoplasms or vascular malformations has been reported.
Global Patient Set
International Patient Summary
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TermSyndroom van Horner
SNOMED CT to Orphanet simple map91413
SNOMED CT to ICD-10 extended map
AdviceALWAYS G90.2
CorrelationSNOMED CT source code to target map code correlation not specified