ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

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

Retinal macular dystrophy type 2

Stargardt disease

Citations in the biomedical literature:

Retinal macular dystrophy type 2		Stargardt disease
	Synonym(s): - MCDR2		Synonym(s): - Fundus flavimaculatus - Macular dystrophy with flecks

	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: (no data available)		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant

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

No signs/symptoms info available.