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Central areolar choroidal dystrophy
3 OMIM references -
2 associated genes
10 connected diseases
No signs/symptoms info
Disease Type of connection
Cone rod dystrophy
Retinitis pigmentosa
Adult-onset foveomacular vitelliform dystrophy
Butterfly-shaped pigment dystrophy
Fundus albipunctatus
Leber congenital amaurosis
Retinitis punctata albescens
Amyotrophic lateral sclerosis
Bradyopsia
Progressive cone dystrophy
Synonym(s):
- Areolar atrophy of the macula
- CACD
- Central areolar choroidal sclerosis
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: no data available
Type of inheritance: autosomal dominant
External references:
3 OMIM references -
1 MeSH reference: C535358
Gene symbol UniProt reference OMIM reference
GUCY2D Q02846600179
PRPH2 P23942179605
No signs/symptoms info available.