ODCs

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

COMMON GENES: 1

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

Fundus albipunctatus

Butterfly-shaped pigment dystrophy

Citations in the biomedical literature:

Fundus albipunctatus		Butterfly-shaped pigment dystrophy

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

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

No signs/symptoms info available.