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Central areolar choroidal dystrophy

3 OMIM references -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
2 signs/symptoms

Central areolar choroidal dystrophy

Bradyopsia

GUCY2D	(UniProt - OMIM)		RGS9	(UniProt - OMIM)
PRPH2	(UniProt - OMIM)		RGS9BP	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GUCY2D	(0.52)	RGS9

Citations in the biomedical literature:

Central areolar choroidal dystrophy		Bradyopsia
	Synonym(s): - Areolar atrophy of the macula - CACD - Central areolar choroidal sclerosis		Synonym(s): - PERRS - Prolonged electroretinal response supression

	Classification (Orphanet): - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease

	Classification (ICD10): - Diseases of the eye and adnexa -		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		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: no data available Type of inheritance: autosomal recessive

	External references: 3 OMIM references - 1 MeSH reference: C535358		External references: 1 OMIM reference - No MeSH references

Bradyopsia
	Very frequent - Mild visual loss / impaired visual acuity - Photophobia
Central areolar choroidal dystrophy
(no data available)