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01 Albinism [NCBI]

Gene


 Gene Link Information
Gain		 01
ADFN [NCBI] 0.00114497
OED [NCBI] 0.000754986
SCAR2 [NCBI] 0.000290167
SCZD2 [NCBI] 0.000275285
TYR [NCBI] 0.000241849
RAB27A [NCBI] 6.73974e-05
FAH [NCBI] 5.58659e-05
OCA2 [NCBI] 3.9002e-05
MYO5A [NCBI] 3.45255e-05
TAT [NCBI] 3.44391e-05
TYRP1 [NCBI] 2.45476e-05
MLPH [NCBI] 2.3263e-05
MITF [NCBI] 2.24856e-05
GPR143 [NCBI] 1.90431e-05
DCT [NCBI] 1.34365e-05
RAB27B [NCBI] 1.31295e-05
PAX6 [NCBI] 1.22498e-05
XG [NCBI] 1.14793e-05
GK [NCBI] 9.87939e-06
LDHA [NCBI] 9.27284e-06
ISL1 [NCBI] 8.34015e-06
HPS1 [NCBI] 7.89595e-06
EDNRB [NCBI] 7.62534e-06
SOX10 [NCBI] 7.27483e-06
SCARB1 [NCBI] 6.47745e-06
PAX2 [NCBI] 6.46338e-06
SPINT2 [NCBI] 6.46338e-06
SERPINF1 [NCBI] 5.03987e-06
CHAT [NCBI] 3.68175e-06
CAT [NCBI] 2.65766e-06
TH [NCBI] 2.59499e-06



OMIM


 OMIM Link Information
gain		 01
ADFN [NCBI] 0.00725736
dilution, pigmentary [NCBI] 0.0030116
OCA1A [NCBI] 0.00221486
immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum [NCBI] 0.00169751
OCA2 [NCBI] 0.00146369
oculocerebral syndrome with hypopigmentation [NCBI] 0.00129172
HPS [NCBI] 0.00127456
TYR [NCBI] 0.00106873
olivopontocerebellar atrophy ii, autosomal recessive [NCBI] 0.000993831
OA1 [NCBI] 0.000724824
AIED [NCBI] 0.000564998
DFN2 [NCBI] 0.000485191
GS2 [NCBI] 0.000420505
OCA1B [NCBI] 0.000379795
abcd syndrome [NCBI] 0.000331004
CHS [NCBI] 0.000285527
tietz syndrome [NCBI] 0.00027649
RAB27A [NCBI] 0.000165813
TYRP1 [NCBI] 0.000154102
SLE [NCBI] 0.000149271
OCA3 [NCBI] 0.000143348
oca2 gene [NCBI] 0.000142292
GS1 [NCBI] 0.000139529
PBT [NCBI] 0.000130226
MITF [NCBI] 0.000111166
albinism-microcephaly-digital anomalies syndrome [NCBI] 0.00011017
OASD [NCBI] 8.77159e-05
deafness, congenital, with total albinism [NCBI] 8.77159e-05
ermine phenotype [NCBI] 8.77159e-05
EDNRB [NCBI] 8.55736e-05
fibrosis of extraocular muscles, congenital, with synergistic divergence [NCBI] 7.92517e-05
albinism, ocular, with sensorineural deafness [NCBI] 7.92517e-05
MLPH [NCBI] 5.68123e-05
WS2A [NCBI] 5.2007e-05
MYO5A [NCBI] 4.68774e-05
SLC45A2 [NCBI] 4.58851e-05
CACNA1F [NCBI] 4.41576e-05
deafness, conductive, with stapes fixation [NCBI] 4.38862e-05
GPX1 [NCBI] 4.20286e-05
IGKC [NCBI] 4.14103e-05
tyrosinemia, type i [NCBI] 2.77244e-05
RHO [NCBI] 2.40268e-05
GJB2 [NCBI] 1.92879e-05
CYP1A1 [NCBI] 1.72594e-05
HSCR1 [NCBI] 1.6719e-05
CHAT [NCBI] 7.28884e-06
CAT [NCBI] 3.125e-06
TS [NCBI] 1.8488e-06
PWS [NCBI] 5.31575e-07



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