Autosomal recessive hereditary disorder	Cone dystrophy	Congenital anomaly of retina	Congenital color blindness	Developmental hereditary disorder
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Achromatopsia (disorder)
	Achromatopsia
	Monochromatism Achromatism
	achromatopsie

Id	56852002
Status	Primitive

Associated morphology	Dystrophy
Finding site	Cone of retina
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	H53.5
Rule	TRUE
Advice	ALWAYS H53.5
Correlation	SNOMED CT source code to target map code correlation not specified

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Complete achromatopsia

Incomplete achromatopsia