Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Erythroblastosis, Fetal [NCBI]

Gene


 Gene Link Information
Gain		 01
RHCE [NCBI] 6.64389e-05
EPO [NCBI] 4.39963e-05
RHD [NCBI] 3.76434e-05
SLC14A1 [NCBI] 3.22518e-05
G6PD [NCBI] 1.90697e-05
KEL [NCBI] 1.53531e-05
ANG [NCBI] 9.62107e-06
DARC [NCBI] 8.89187e-06
TFPI2 [NCBI] 7.99028e-06
SRY [NCBI] 6.96815e-06
UGT1A1 [NCBI] 6.13685e-06
ACHE [NCBI] 3.79689e-06
AVP [NCBI] 3.76138e-06
VEGFA [NCBI] 2.74257e-06
PTH [NCBI] 2.0038e-06



OMIM


 OMIM Link Information
gain		 01
skin creases, multiple benign ring-shaped, of limbs [NCBI] 0.0010375
EPO [NCBI] 0.000159039
DI [NCBI] 0.000157129
RD [NCBI] 0.000157129
SC [NCBI] 0.000134657
crigler-najjar syndrome [NCBI] 8.90891e-05
KEL [NCBI] 7.43456e-05
CD55 [NCBI] 6.91455e-05
thrombasthenia of glanzmann and naegeli [NCBI] 6.81454e-05
G6PD [NCBI] 6.41078e-05
RHD [NCBI] 5.69272e-05
FY [NCBI] 4.68337e-05
polycystic kidneys [NCBI] 4.48257e-05
TFPI2 [NCBI] 4.42512e-05
HBD [NCBI] 4.2474e-05
HBB [NCBI] 1.52741e-05
ACHE [NCBI] 8.78161e-06
AVP [NCBI] 6.37111e-06
PTH [NCBI] 1.45757e-06
VEGF [NCBI] 5.93696e-08



Database Center for Life Science