Autosomal dominant hereditary disorder	Chronic disease	Hereditary macular dystrophy
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Occult macular dystrophy (disorder)
	Occult macular dystrophy
	OCMD - occult macular dystrophy OMD - occult macular dystrophy
	A rare genetic retinal dystrophy disease with characteristics of bilateral progressive decline of visual acuity due to retinal dysfunction confined only to the macula, associated with normal fundus and fluorescein angiograms and severly attenuated focal macular and multifocal electroretinograms. There is evidence the disease is caused by heterozygous mutation in the RP1L1 gene on chromosome 8p23.
	occulte maculadystrofie

Id	770667002
Status	Primitive

Clinical course

Associated morphology	Dystrophy
Finding site	Macula lutea structure

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	H35.5
Rule	TRUE
Advice	ALWAYS H35.5
Correlation	SNOMED CT source code to target map code correlation not specified