Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Oculocerebrorenal Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
OCRL [NCBI] 0.000941628
INPP5D [NCBI] 0.000110751
INPP4B [NCBI] 1.38369e-05
INPP4A [NCBI] 1.29385e-05
CLCN6 [NCBI] 1.29385e-05
INPP1 [NCBI] 1.23551e-05
INPP5A [NCBI] 1.23551e-05
APPL1 [NCBI] 1.19214e-05
GOLGA5 [NCBI] 1.19214e-05
CLTC [NCBI] 1.06362e-05
TGOLN2 [NCBI] 1.04643e-05
CLCN5 [NCBI] 8.69247e-06
CETP [NCBI] 8.48563e-06
CDC42 [NCBI] 7.67343e-06
CUBN [NCBI] 7.61068e-06
RAC1 [NCBI] 5.93316e-06
GRB2 [NCBI] 5.23373e-06
AMBP [NCBI] 4.77144e-06
RET [NCBI] 3.61969e-06
PTH [NCBI] 8.05212e-07



OMIM


 OMIM Link Information
gain		 01
OCRL [NCBI] 0.00277976
x inactivation, familial skewed, 2 [NCBI] 0.00137383
OCRL [NCBI] 0.00104025
dent disease 2 [NCBI] 0.000132242
hypomagnesemia, renal, with ocular involvement [NCBI] 0.000101296
COPB [NCBI] 9.22788e-05
INPP5A [NCBI] 9.22788e-05
pierson syndrome [NCBI] 7.95849e-05
GOLGA5 [NCBI] 7.32984e-05
dent disease 1 [NCBI] 7.16717e-05
RAC1 [NCBI] 5.80724e-05
NS1 [NCBI] 4.22312e-05
PTH [NCBI] 3.73935e-06



Database Center for Life Science