Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Properdin	[NCBI]

Gene	Link	Information Gain
CFP	[NCBI]	7.88919e-05
C3	[NCBI]	1.90951e-05
CFB	[NCBI]	1.64627e-05
C4B	[NCBI]	5.98121e-06
THBS1	[NCBI]	3.31891e-06
HEPACAM	[NCBI]	2.31698e-06
HSD17B6	[NCBI]	2.28719e-06
B3GALTL	[NCBI]	2.23604e-06
CFD	[NCBI]	2.17399e-06
SEMA5A	[NCBI]	2.12367e-06
BCAT1	[NCBI]	2.06859e-06
C4BPB	[NCBI]	2.01264e-06
CTNND2	[NCBI]	2.00273e-06
C9	[NCBI]	1.94207e-06
THBS2	[NCBI]	1.92699e-06
SFRP4	[NCBI]	1.86804e-06
C2	[NCBI]	1.84015e-06
C4BPA	[NCBI]	1.77889e-06
C4A	[NCBI]	1.75092e-06
C5	[NCBI]	1.74344e-06
C5AR1	[NCBI]	1.6812e-06
CD55	[NCBI]	1.63076e-06
C3AR1	[NCBI]	1.59461e-06
FGA	[NCBI]	1.51798e-06
ITGAM	[NCBI]	1.45852e-06
CFH	[NCBI]	1.40993e-06
CYP1B1	[NCBI]	1.40058e-06
MAOA	[NCBI]	1.38665e-06
TLR3	[NCBI]	1.31785e-06
MMP2	[NCBI]	1.17926e-06
CD46	[NCBI]	1.15999e-06
MMP9	[NCBI]	1.13329e-06

OMIM	Link	Information gain
properdin deficiency, x-linked	[NCBI]	0.00301229
IGAN1	[NCBI]	0.0019383
PFC	[NCBI]	0.000698808
CFB	[NCBI]	0.000303913
cirrhosis, familial	[NCBI]	0.000125861
cri-du-chat syndrome	[NCBI]	0.000118131
membranoproliferative glomerulonephritis, x-linked	[NCBI]	0.000118131
complement factor i deficiency	[NCBI]	9.79128e-05
complement component 2 deficiency	[NCBI]	8.67144e-05
complement component 7 deficiency	[NCBI]	8.15665e-05
SLE	[NCBI]	7.26014e-05
SCIDX1	[NCBI]	7.05973e-05
C4B	[NCBI]	5.1755e-05
C4A	[NCBI]	5.15348e-05
SEMA5A	[NCBI]	3.13477e-05
SYN1	[NCBI]	3.13477e-05
CFI	[NCBI]	2.38602e-05
TIMP1	[NCBI]	2.35597e-05
C3	[NCBI]	2.08693e-05
MMP2	[NCBI]	2.01326e-05
MBL2	[NCBI]	1.16234e-05
RA	[NCBI]	6.75645e-06
AVP	[NCBI]	9.0489e-07
AD	[NCBI]	5.38392e-09