Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 IgG Deficiency [NCBI]

Gene


 Gene Link Information
Gain		 01
HLA-A [NCBI] 1.99573e-05
HLA-B [NCBI] 1.9128e-05
ENPP3 [NCBI] 1.27529e-05
CIITA [NCBI] 9.60671e-06
TAP1 [NCBI] 8.92659e-06
NBN [NCBI] 8.79429e-06
HFE [NCBI] 6.52783e-06



OMIM


 OMIM Link Information
gain		 01
CVID [NCBI] 0.000784967
dandy-walker-like malformation with atrioventricular septal defect [NCBI] 0.000749926
IGAD1 [NCBI] 0.000734606
HIGM1 [NCBI] 0.000323176
IGHG2 [NCBI] 0.000200768
enteropathy, familial, with villous edema and immunoglobulin g2 deficiency [NCBI] 0.000131618
CHH [NCBI] 0.00011603
agammaglobulinemia, non-bruton type, autosomal recessive [NCBI] 8.5109e-05
IGHG3 [NCBI] 8.05705e-05
AT [NCBI] 6.74928e-05
PAX5 [NCBI] 6.53402e-05
IGHG1 [NCBI] 5.78247e-05
A2M [NCBI] 5.2356e-05
IP [NCBI] 3.63557e-05
MBL2 [NCBI] 3.52488e-05
RA [NCBI] 3.28911e-05
SLE [NCBI] 1.76805e-07



Database Center for Life Science