All diseases

OMIM ID
609814
OMIM term:
COMPLEMENT FACTOR H DEFICIENCY; CFHD
Alternative terms:
FACTOR H DEFICIENCY
CFH DEFICIENCY
(∗) Location:
1q31.3  
(†) Associated OMIM genes:
CFH  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/1zq2g9hm