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Items: 2

1.

Choroidal dystrophy, central areolar, 1

Any central areolar choroidal dystrophy in which the cause of the disease is a mutation in the GUCY2D gene. [from MONDO]

MedGen UID:
1639900
Concept ID:
C4551884
Disease or Syndrome
2.

Central areolar choroidal dystrophy

A hereditary macular disorder, usually presenting between the ages of 30-60, characterized by a large area of atrophy in the centre of the macula and the loss or absence of photoreceptors, retinal pigment epithelium and choriocapillaris in this area, resulting in a progressive decrease in visual acuity. [from ORDO]

MedGen UID:
283932
Concept ID:
C1536451
Disease or Syndrome

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