Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hypoaldosteronism [NCBI]

Gene


 Gene Link Information
Gain		 01
CYP11B2 [NCBI] 5.20569e-05
SLC4A4 [NCBI] 1.3485e-05
SCNN1B [NCBI] 1.13948e-05
SLC12A3 [NCBI] 1.0857e-05
SLC9A3 [NCBI] 9.76586e-06
PTH [NCBI] 4.31111e-06



OMIM


 OMIM Link Information
gain		 01
hyperreninemic hypoaldosteronism, familial, 2 [NCBI] 0.00159179
corticosterone methyloxidase type ii deficiency [NCBI] 0.000354253
CYP11B2 [NCBI] 0.000136143
cortisol 11-beta-ketoreductase deficiency [NCBI] 0.000110801
liddle syndrome [NCBI] 9.63076e-05
PHA2 [NCBI] 8.77542e-05
SCNN1A [NCBI] 6.724e-05
IL6 [NCBI] 4.17052e-05
ALD [NCBI] 3.82965e-05
FMF [NCBI] 3.22336e-05
PTH [NCBI] 9.14044e-06
SLE [NCBI] 1.36693e-08



Database Center for Life Science