autosomaal dominante hereditaire aandoening	congenitale afwijking van oog	hereditaire aandoening van visueel systeem	hereditaire ontwikkelingsstoornis
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SOX2-anoftalmie (aandoening)
	SOX2-anoftalmie
	SOX2 anophthalmia syndrome
	AEG - anophthalmia-esophageal-genital syndrome SOX2-related eye disorder Anophthalmia-esophageal-genital syndrome Syndromic microphthalmia 3

Id	698851003
Status	Primitive

Associated morphology	afwijkend klein
Finding site	structuur van bulbus oculi
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

SNOMED CT to Orphanet simple map

77298

SNOMED CT to ICD-10 extended map

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified