Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Acatalasia [NCBI]

Gene


 Gene Link Information
Gain		 01
CAT [NCBI] 5.76682e-05
CCL3 [NCBI] 1.02426e-05
ESD [NCBI] 9.9252e-06
MPO [NCBI] 4.74906e-06



OMIM


 OMIM Link Information
gain		 01
WT1 [NCBI] 0.000264635
CAT [NCBI] 0.000260298
mental and growth retardation with amblyopia [NCBI] 0.000134657
d-bifunctional protein deficiency [NCBI] 9.75849e-05
refsum disease, infantile form [NCBI] 8.78187e-05
AN2 [NCBI] 7.73868e-05
adrenoleukodystrophy, autosomal neonatal form [NCBI] 7.6759e-05
MPO [NCBI] 1.37718e-05



Database Center for Life Science