ODCs

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

COMMON GENES: 1

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

Complement component 3 deficiency

Atypical hemolytic uremic syndrome with C3 anomaly

Citations in the biomedical literature:

Complement component 3 deficiency		Atypical hemolytic uremic syndrome with C3 anomaly
	Synonym(s): - C3 deficiency		Synonym(s): - Atypical HUS with C3 anomaly - D-HUS with C3 anomaly - Hemolytic-uremic syndrome without diarrhea with C3 anomaly - aHUS with C3 anomaly

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

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

No signs/symptoms info available.