Retinitis Pigmentosa 19

Alternative Names

  • RP19
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WHO-ICD-10 version:2010

Diseases of the eye and adnexa

Disorders of choroid and retina

OMIM Number

601718

Mode of Inheritance

Autosomal recessive

Gene Map Locus

1p22.1

Description

Retinitis pigmentosa (RP) refers to a heterogeneous group of inherited ocular diseases that result in a progressive retinal degeneration affecting 1 in 3,000 to 5,000 people. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
601718.G.1SyriaUnknownYesYes Visual impairment; Rod-cone dystrophy... NM_000350.3:c.3482G>AHeterozygousAutosomal, RecessivePatel et al, 2018 4 members of a famil...
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