ODCs

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

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

Familial drusen

Dense deposit disease

CFH	(UniProt - OMIM)		CFH	(UniProt - OMIM)
EFEMP1	(UniProt - OMIM)		CFHR1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CFH	(0.62)	CFHR1

Citations in the biomedical literature:

Familial drusen		Dense deposit disease
	Synonym(s): - DHRD - Dominant drusen - Dominant radial drusen - Doyne honeycomb retinal dystrophy - Malattia leventinese		Synonym(s): - Membranoproliferative glomerulonephritis type 2

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

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D015432

No signs/symptoms info available.