- OMIM ID
-
312060
- OMIM term:
- PROPERDIN DEFICIENCY, X-LINKED; CFPD
- Alternative terms:
-
PROPERDIN P FACTOR DEFICIENCY; PFD
COMPLEMENT FACTOR PROPERDIN DEFICIENCY
PROPERDIN DEFICIENCY, TYPE I PROPERDIN DEFICIENCY, TYPE II, INCLUDED
PROPERDIN DEFICIENCY, TYPE III, INCLUDED
- (∗) Location:
- Xp11.23
- (†) Associated OMIM genes:
- CFP
- (‡) Associated MGI genes:
Loading mouse genes ...