Autosomal dominant hereditary disorder	Congenital anomaly of eye	Developmental hereditary disorder	Hereditary disorder of the visual system
\|	\|	\|	\|

SOX2 anophthalmia syndrome (disorder)
	SOX2 anophthalmia syndrome
	AEG - anophthalmia-esophageal-genital syndrome SOX2-related eye disorder Anophthalmia-esophageal-genital syndrome Syndromic microphthalmia 3
	SOX2-anoftalmie

Id	698851003
Status	Primitive

Associated morphology	Congenital smallness
Finding site	Eye structure
Occurrence	Congenital
Pathological process	Pathological developmental process

ICD-10 complex map reference set

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