ODCs

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1 OMIM reference -
3 associated genes
No signs/symptoms info

COMMON GENES: 1

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

Fundus albipunctatus

Central areolar choroidal dystrophy

Citations in the biomedical literature:

Fundus albipunctatus		Central areolar choroidal dystrophy
	Synonym(s): (no synonyms)		Synonym(s): - Areolar atrophy of the macula - CACD - Central areolar choroidal sclerosis

	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: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		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: 1 OMIM reference - No MeSH references		External references: 3 OMIM references - 1 MeSH reference: C535358

No signs/symptoms info available.