ODCs

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

COMMON GENES: 1

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

Familial drusen

Immunodeficiency with factor H anomaly

CFH	(UniProt - OMIM)		CFH	(UniProt - OMIM)
EFEMP1	(UniProt - OMIM)

Citations in the biomedical literature:

Familial drusen		Immunodeficiency with factor H anomaly
	Synonym(s): - DHRD - Dominant drusen - Dominant radial drusen - Doyne honeycomb retinal dystrophy - Malattia leventinese		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.