Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Tay-Sachs Disease [NCBI]

Gene


 Gene Link Information
Gain		 01
HEXA [NCBI] 0.00115551
HEXB [NCBI] 0.000154506
PSAP [NCBI] 8.46312e-05
GM2A [NCBI] 3.47844e-05
TPP1 [NCBI] 5.73098e-06
BRCA1 [NCBI] 2.30636e-06
CFTR [NCBI] 6.77819e-07



OMIM


 OMIM Link Information
gain		 01
TSD [NCBI] 0.0158499
HEXA [NCBI] 0.00556879
gangliosidosis, gm2, type iii, or juvenile type [NCBI] 0.00123814
sandhoff disease [NCBI] 0.000562321
HEXB [NCBI] 0.000281486
tay-sachs disease, ab variant [NCBI] 0.00020219
CF [NCBI] 0.000105296
gangliosidosis, gm2, juvenile, a(m)b variant [NCBI] 0.000102119
osteopetrosis and infantile neuroaxonal dystrophy [NCBI] 7.1224e-05
CLN10 [NCBI] 6.57453e-05
gaucher disease, type i [NCBI] 5.54158e-05
metachromatic leukodystrophy due to saposin b deficiency [NCBI] 4.80949e-05
INAD1 [NCBI] 4.00182e-05
CLN2 [NCBI] 3.67994e-05
gm1-gangliosidosis, type i [NCBI] 3.04275e-05
NDP [NCBI] 2.88221e-05
HSAN3 [NCBI] 2.47214e-05
GBA [NCBI] 2.0372e-05
metachromatic leukodystrophy [NCBI] 1.80418e-05
BRCA1 [NCBI] 1.24317e-05
phenylketonuria [NCBI] 1.15764e-05



Database Center for Life Science