Autosomal dominant hereditary disorder	Congenital abnormality of lacrimal drainage system	Congenital anomaly of eyelid	Congenital stenosis	Dacryocystitis	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Hereditary disorder of the visual system	Osteopoikilosis	Stenosis of lacrimal canaliculi
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Dacryocystitis and osteopoikilosis syndrome (disorder)
	Dacryocystitis and osteopoikilosis syndrome
	Gunal Seber Basaran syndrome
	An exceedingly rare autosomal dominant disorder reported in only a few patients to date with characteristics of dacryocystitis due to lacrimal canal stenosis and osteopoikilosis (demonstrated radiologically as discrete spherical osteosclerotic lesions of 2-10 mm in diameter).
	syndroom van dacryocystitis en osteopoikilie
	syndroom van traanzakontsteking en osteopoikilie syndroom van Gunal-Seber-Basaran

Id	721082002
Status	Defined

Associated morphology	Inflammatory morphology
Finding site	Lacrimal sac structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Stenosis
Finding site	Lacrimal canaliculus structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Dysplasia
Finding site	Bone structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Above reference range
Interprets	Bone density scan

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	H04.3
Rule	TRUE
Advice	ALWAYS H04.3
Correlation	SNOMED CT source code to target map code correlation not specified

Target	Q10.5
Rule	TRUE
Advice	ALWAYS Q10.5
Correlation	SNOMED CT source code to target map code correlation not specified

Target	Q78.8
Rule	TRUE
Advice	ALWAYS Q78.8
Correlation	SNOMED CT source code to target map code correlation not specified