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Summary Literature (0)
MIM:609814 - COMPLEMENT FACTOR H DEFICIENCY; CFHD

Xenbase Genes: cfh

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012350 - complement factor H deficiency
MONDO:0016061 - immunodeficiency with factor H anomaly
MONDO:0016244 - atypical hemolytic-uremic syndrome
MONDO:0018013 - non-immunoglobulin-mediated membranoproliferative glomerulonephritis
MONDO:0018904 - primary membranoproliferative glomerulonephritis
MONDO:0019736 - dense deposit disease
MONDO:0019738 - atypical hemolytic-uremic syndrome with H factor anomaly