Congenital disease	Corneal endothelial dystrophy	Hereditary corneal dystrophy	X-linked recessive hereditary disease
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X-linked endothelial dystrophy of cornea (disorder)
	X-linked endothelial corneal dystrophy
	X-linked endothelial dystrophy of cornea
	A rare subtype of posterior corneal dystrophy with characteristics of congenital ground glass corneal clouding or a diffuse corneal haze, and blurred vision in male patients. Prevalence of this rare corneal dystrophy is unknown. Males are affected more severely than females. The condition is progressive in males and non-progressive in females. Has been mapped to the long arm of the X-chromosome (Xq25) but the causative gene has not been identified. Transmission is X-linked recessive.
	X-gebonden endotheliale corneadystrofie
	X-gebonden cornea-endotheeldystrofie X-gebonden endotheeldystrofie van hoornvlies

Id	718579008
Status	Primitive

Associated morphology	Dystrophy
Finding site	Structure of corneal endothelium
Occurrence	Congenital

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	H18.5
Rule	TRUE
Advice	ALWAYS H18.5
Correlation	SNOMED CT source code to target map code correlation not specified