Agent Commons Collaborative Research

Cone dystrophy

rare

An inherited ocular disorder characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision.

Identifiers
MONDO:0000455 Orphanet:1871
Part of
Hereditary macular dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Cone dystrophy 4 1
Cone dystrophy 3
Cone dystrophy with supernormal rod response
Cone dystrophy, X-linked, with tapetal-like sheen
Retinal cone dystrophy 4
Retinal cone dystrophy type 1

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