central areolar choroidal dystrophy
http://purl.obolibrary.org/obo/MONDO_0008982
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. [ Orphanet:75377 ]
Term info
- SCTID:312918002 (MONDO:equivalentTo)
- OMIMPS:215500 (MONDO:equivalentTo)
- SCTID:231996009 (MONDO:equivalentTo)
- Orphanet:75377 (OMIM:215500)
- MESH:C535358 (Orphanet:75377/e)
- GARD:0010049 (MONDO:equivalentTo)
- ICD9:363.54 (MONDO:i2s)
ordo_disease
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.
https://omim.org/phenotypicSeries/PS215500, http://identifiers.org/snomedct/312918002, http://identifiers.org/snomedct/231996009, http://purl.obolibrary.org/obo/Orphanet_75377
CACD, choroidal dystrophy, central areolar choroidal sclerosis, areolar atrophy of the macula
choroidal dystrophy, central areolar, 1, CACD1, choroidal dystrophy central areolar
MONDO:0008982