ODCs

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

PROTEIN INTERACTIONS: 1

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

Atypical hemolytic uremic syndrome with I factor anomaly

Dense deposit disease

CFI	(UniProt - OMIM)		CFH	(UniProt - OMIM)
			CFHR1	(UniProt - OMIM)


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

Citations in the biomedical literature:

Atypical hemolytic uremic syndrome with I factor anomaly		Dense deposit disease
	Synonym(s): - Atypical HUS with I factor anomaly - D-HUS with I factor anomaly - Hemolytic-uremic syndrome without diarrhea with I factor anomaly - aHUS with I factor anomaly		Synonym(s): - Membranoproliferative glomerulonephritis type 2

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

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): (no data available)

	Epidemiological data: (no data available)		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: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D015432

No signs/symptoms info available.