autosomaal dominante hereditaire aandoening	Robinow-syndroom
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autosomaal dominant Robinow-syndroom (aandoening)
	autosomaal dominant Robinow-syndroom
	autosomaal dominant syndroom van Robinow
	Autosomal dominant Robinow syndrome
	The more common type of Robinow syndrome characterized by mild to moderate limb shortening and abnormalities of the head, face and external genitalia.

Id	890233009
Status	Defined

Associated morphology	dysplasie
Finding site	botstructuur van extremiteit
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

Has interpretation	onder referentiebereik
Interprets	Limb length

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

SNOMED CT to ICD-10 extended map

Target	Q87.1
Rule	TRUE
Advice	ALWAYS Q87.1 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified