Progressive cone dystrophy (Q99749): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Transtorno ocular hereditário progressivo caracterizado por perda de cones, os fotorreceptores responsáveis pela visão central e colorida. | |||
| description / en | description / en | ||
This is a progressive inherited ocular disorder characterised by the loss of cone cells, the photoreceptors responsible for both central and colour vision. | |||
Revision as of 16:25, 16 August 2026
This is a progressive inherited ocular disorder characterised by the loss of cone cells, the photoreceptors responsible for both central and colour vision.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_952706927 |
||
| English | Progressive cone dystrophy |
This is a progressive inherited ocular disorder characterised by the loss of cone cells, the photoreceptors responsible for both central and colour vision. |
