autosomaal recessieve hereditaire aandoening	congenitale obstructie van ductus nasolacrimalis	familiaire aandoening	hereditaire aandoening van visueel systeem	hereditaire ontwikkelingsstoornis
\|	\|	\|	\|	\|

familiaire congenitale stenose van ductus nasolacrimalis (aandoening)
	familiaire congenitale stenose van ductus nasolacrimalis
	familiale congenitale obstructie van neustraankanaal
	Familial congenital nasolacrimal duct obstruction
	A rare, genetic, otorhinolaryngological malformation characterized by congenital impatency of the nasolacrimal drainage system in various members of a family. Presentation is not specific and may include a uni- or bilateral medial canthal mass, dacryocystitis, nasal obstruction, periorbital cellulitis, and epiphora. Dacryocystocele and lacrimal puncta agenesis may be associated.

Id	1230016009
Status	Defined

Associated morphology	obstructie
Finding site	structuur van ductus nasolacrimalis
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

SNOMED CT to Orphanet simple map

451612

SNOMED CT to ICD-10 extended map

Target	Q10.5
Rule	TRUE
Advice	ALWAYS Q10.5 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified