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Fig. 3 | Orphanet Journal of Rare Diseases

Fig. 3

From: Design, development and deployment of a web-based interoperable registry for inherited retinal dystrophies in Portugal: the IRD-PT

Fig. 3

Graphical representation of the relative frequency of each clinical diagnosis in the 537 patients included in the IRD-PT registry. Those with < 1% cases are expressed under the tag Other. RP retinitis pigmentosa, PXE pseudoxanthoma elasticum, ADOA autosomal dominant optic atrophy, PPRCA pigmented paravenous retinochoroidal atrophy, CACD central areolar choroidal dystrophy

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172