autosomaal recessieve hereditaire aandoening	sotossyndroom
\|	\|

'APC regulator of Wnt signaling pathway 2'-gerelateerd sotossyndroom (aandoening)
	APC2-gerelateerd sotossyndroom
	sotossyndroom door mutatie in APC2-gen APC2-gerelateerd Sotos-syndroom 'APC regulator of Wnt signaling pathway 2'-gerelateerd sotossyndroom syndroom van Sotos door mutatie in APC2-gen
	APC2 gene related Sotos syndrome
	APC regulator of Wnt signaling pathway 2 gene related Sotos syndrome

Id	1402127002
Status	Primitive

Finding site

structuur van encephalon

Has interpretation	gestoord
Interprets	intellectueel vermogen

Has interpretation	gestoord
Interprets	Adaptation behavior

Has interpretation	boven referentiebereik
Interprets	meetbare observatie betreffende lengte en/of groei

Has interpretation	boven referentiebereik
Interprets	hoofdomtrek

Associated morphology	dysplasie
Finding site	structuur van skeletstelsel
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	morfologische afwijking
Finding site	structuur van aangezicht
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

SNOMED CT to ICD-10 extended map

Target	Q87.3
Rule	TRUE
Advice	ALWAYS Q87.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified