Autosomal dominant hereditary disorder	Congenital absence of salivary gland	Congenital anomaly of lacrimal gland	Congenital aplasia of lacrimal structure	Developmental hereditary disorder	Digestive system hereditary disorder	Hereditary disorder of the visual system
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Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder)
	Aplasia of lacrimal and salivary gland
	Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland
	A rare autosomal dominant disorder with features of aplasia, atresia or hypoplasia of the lacrimal and salivary glands leading to varying manifestations from infancy such as recurrent eye infections, irritable eyes, epiphora, xerostomia, dental caries, dental erosion and oral inflammation.
	congenitale aplasie van traanklier gelijktijdig met congenitale aplasie van speekselklier
	aplasie van traan- en speekselklieren

Id	715656004
Status	Defined

Associated morphology	Aplasia
Finding site	Salivary gland structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Aplasia
Finding site	Lacrimal gland structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q10.4
Rule	TRUE
Advice	ALWAYS Q10.4
Correlation	SNOMED CT source code to target map code correlation not specified

Target	Q38.4
Rule	TRUE
Advice	ALWAYS Q38.4
Correlation	SNOMED CT source code to target map code correlation not specified