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MeSH keywords -> Related genes, diseases (OMIM)


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01 Anemia, Dyserythropoietic, Congenital [NCBI]

Gene


 Gene Link Information
Gain		 01
CDAN2 [NCBI] 0.000817003
CDAN3 [NCBI] 0.000401057
STRCP [NCBI] 0.000401057
HISPPD2B [NCBI] 0.000401057
CATSPER2P1 [NCBI] 0.000340315
CDAN1 [NCBI] 9.48259e-05
LPIN2 [NCBI] 2.85955e-05
ZSCAN29 [NCBI] 1.87183e-05
CEP27 [NCBI] 1.87183e-05
GATA1 [NCBI] 1.81071e-05
HISPPD2A [NCBI] 1.63379e-05
TMEM62 [NCBI] 1.63379e-05
CATSPER2 [NCBI] 1.63379e-05
ZFP106 [NCBI] 1.63379e-05
TMEM87A [NCBI] 1.63379e-05
TGM5 [NCBI] 1.54394e-05
MAN2A1 [NCBI] 1.44221e-05
TTBK2 [NCBI] 1.44221e-05
GANC [NCBI] 1.37888e-05
MGAT2 [NCBI] 1.33275e-05
CCNDBP1 [NCBI] 1.29644e-05
EPB42 [NCBI] 1.26649e-05
UBR1 [NCBI] 1.25327e-05
SNAP23 [NCBI] 1.241e-05
ZFPM1 [NCBI] 1.2087e-05
STOM [NCBI] 1.14407e-05
EPB41L1 [NCBI] 8.66663e-06
EPB41L2 [NCBI] 8.48948e-06
HFE [NCBI] 4.77251e-06
EPO [NCBI] 3.77864e-06



OMIM


 OMIM Link Information
gain		 01
CDAN2 [NCBI] 0.0131278
CDAN3 [NCBI] 0.00316599
anemia, dyserythropoietic congenital, type i [NCBI] 0.00175675
CDAN1 [NCBI] 0.000458079
majeed syndrome [NCBI] 0.000360291
dyserythropoiesis, congenital, with internuclear chromatin bridges and ultrastructurally normal erythroblast heterochromatin [NCBI] 0.00026386
deafness, sensorineural, and male infertility [NCBI] 0.00023291
LPIN2 [NCBI] 0.00022015
dyserythropoietic anemia with thrombocytopenia [NCBI] 0.000218924
CDG2A [NCBI] 0.00018661
AQP1 [NCBI] 0.000171016
CATSPER2 [NCBI] 0.000153629
STRC [NCBI] 0.00014774
GATA1 [NCBI] 0.000113662
congenital disorder of glycosylation, type i/iix [NCBI] 8.5109e-05
CDG1B [NCBI] 7.89629e-05
MAN2A1 [NCBI] 7.65036e-05
ZFPM1 [NCBI] 7.13032e-05
CDG1A [NCBI] 5.27128e-05
CRMO [NCBI] 4.81669e-05
ALPS [NCBI] 4.03848e-05
SLC4A1 [NCBI] 3.99572e-05
DBA [NCBI] 3.81717e-05
FMF [NCBI] 1.39424e-05
G6PD [NCBI] 1.27782e-05
EPO [NCBI] 6.06677e-06



Database Center for Life Science