Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 WAGR Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
PAX6 [NCBI] 0.000124103
MPPED2 [NCBI] 5.47184e-05
MPPED1 [NCBI] 3.63944e-05
BDNF [NCBI] 1.8759e-05
LUZP2 [NCBI] 1.57758e-05
ALMS1 [NCBI] 1.07494e-05
ALDH5A1 [NCBI] 9.60764e-06
WT1 [NCBI] 7.62235e-06
RAG1 [NCBI] 6.20878e-06
CTNNB1 [NCBI] 3.5512e-06



OMIM


 OMIM Link Information
gain		 01
wagr syndrome [NCBI] 0.00113301
potocki-shaffer syndrome [NCBI] 0.000205256
C11ORF8 [NCBI] 0.000195008
WT1 [NCBI] 0.000109998
PAX6 [NCBI] 0.000108208
C22ORF1 [NCBI] 9.68811e-05
LUZP2 [NCBI] 9.68811e-05
exostoses, multiple, type ii [NCBI] 8.76406e-05
succinic semialdehyde dehydrogenase deficiency [NCBI] 8.66284e-05
ALX4 [NCBI] 6.83464e-05
WT1 [NCBI] 5.79608e-05
BDNF [NCBI] 4.95146e-05



Database Center for Life Science