ODCs

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

COMMON GENES: 1

2 OMIM references -
1 associated gene
No signs/symptoms info

Central areolar choroidal dystrophy

Butterfly-shaped pigment dystrophy

GUCY2D	(UniProt - OMIM)		PRPH2	(UniProt - OMIM)
PRPH2	(UniProt - OMIM)

Citations in the biomedical literature:

Central areolar choroidal dystrophy		Butterfly-shaped pigment dystrophy
	Synonym(s): - Areolar atrophy of the macula - CACD - Central areolar choroidal sclerosis		Synonym(s): (no synonyms)

	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: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 3 OMIM references - 1 MeSH reference: C535358		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.