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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hypopigmentation [NCBI]

Gene


 Gene Link Information
Gain		 01
DUH [NCBI] 0.000707371
HMI [NCBI] 0.000317391
RAB27A [NCBI] 5.74415e-05
MITF [NCBI] 5.60829e-05
DCT [NCBI] 5.56814e-05
SOX10 [NCBI] 5.36931e-05
MYO5A [NCBI] 5.06364e-05
EDNRB [NCBI] 3.04603e-05
OCA2 [NCBI] 2.94584e-05
AP3B1 [NCBI] 2.285e-05
GPR143 [NCBI] 2.02091e-05
TYR [NCBI] 1.65848e-05
TYRP1 [NCBI] 1.60987e-05
RAB27B [NCBI] 1.37072e-05
ZMYM3 [NCBI] 1.37072e-05
SLC24A5 [NCBI] 1.37072e-05
HPS6 [NCBI] 1.31238e-05
FIG4 [NCBI] 1.18108e-05
BLOC1S2 [NCBI] 1.14046e-05
MLPH [NCBI] 1.09332e-05
HPS3 [NCBI] 1.08011e-05
EBP [NCBI] 9.34737e-06
PRM2 [NCBI] 8.83396e-06
HPS1 [NCBI] 8.47195e-06
FTL [NCBI] 8.43963e-06
HCFC1 [NCBI] 8.25762e-06
DTNBP1 [NCBI] 8.04168e-06
ADAR [NCBI] 7.91939e-06
POU2F1 [NCBI] 7.8053e-06
GZMA [NCBI] 7.21451e-06
SNRPN [NCBI] 7.05108e-06
PAX3 [NCBI] 5.91756e-06
PAH [NCBI] 5.14836e-06
MSH2 [NCBI] 3.14221e-06
CD68 [NCBI] 2.94212e-06



OMIM


 OMIM Link Information
gain		 01
focal facial dermal dysplasia [NCBI] 0.00102023
oculocerebral syndrome with hypopigmentation [NCBI] 0.000900049
facial ectodermal dysplasia [NCBI] 0.000807657
HPS [NCBI] 0.000421387
TS [NCBI] 0.000281404
MITF [NCBI] 0.000257405
GS3 [NCBI] 0.000249889
dyschromatosis symmetrica hereditaria 1 [NCBI] 0.000221073
yemenite deaf-blind hypopigmentation syndrome [NCBI] 0.000218941
MYO5A [NCBI] 0.000203683
SOX10 [NCBI] 0.00017324
GS1 [NCBI] 0.000168827
AS [NCBI] 0.000153057
MLPH [NCBI] 0.000148218
DDD [NCBI] 0.000141388
raindrop hypopigmentation [NCBI] 0.000124742
CHS [NCBI] 0.000124075
AP3B1 [NCBI] 0.00012031
PWS [NCBI] 0.000108168
abcd syndrome [NCBI] 9.38016e-05
halo nevi [NCBI] 9.38016e-05
TYR [NCBI] 8.61715e-05
tietz syndrome [NCBI] 8.42118e-05
HSCR1 [NCBI] 8.16263e-05
elejalde disease [NCBI] 7.59315e-05
OCA3 [NCBI] 7.39071e-05
ZNF261 [NCBI] 7.38721e-05
GS2 [NCBI] 6.90246e-05
HPS3 [NCBI] 6.86721e-05
MADA [NCBI] 5.62135e-05
SLC45A2 [NCBI] 5.43545e-05
ZNF198 [NCBI] 5.3451e-05
HPS1 [NCBI] 5.3451e-05
PKS [NCBI] 5.23321e-05
RAB27A [NCBI] 5.18591e-05
OCA2 [NCBI] 4.96293e-05
OCA1A [NCBI] 4.8056e-05
FDH [NCBI] 4.73251e-05
oca2 gene [NCBI] 4.44511e-05
EDNRB [NCBI] 4.41096e-05
RTS [NCBI] 4.38244e-05
OA1 [NCBI] 4.14755e-05
HMI [NCBI] 3.98249e-05
KITLG [NCBI] 3.68524e-05
homocystinuria [NCBI] 3.13671e-05
MEN1 [NCBI] 3.0251e-05
BCNS [NCBI] 2.64693e-05
lymphoma, non-hodgkin, familial [NCBI] 6.15939e-06



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