3billion
back to listBack to List

CFB

complement factor B

HCNC Approved Symbol
CFB (HGNC:1037)
Genomic Coordinates
6:31,946,095 - 31,952,084 (6p21.33)
Synonyms
H2-Bf, BFD, BF
Disease Associations
This gene is associated with the following 3 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Complement factor B deficiency
615561AR
{Hemolytic uremic syndrome, atypical, susceptibility to, 4}
612924AD
{Macular degeneration, age-related, 14, reduced risk of}
615489DD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the CFB gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results