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MeSH keywords -> Related genes, diseases (OMIM)


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01 Waardenburg Syndrome [NCBI]


Gene


Gene Link Information
Gain
01
PAX3 [NCBI] 0.000828808
MITF [NCBI] 0.000523694
WS2B [NCBI] 0.000499621
WS2A [NCBI] 0.000499621
SOX10 [NCBI] 0.000407799
EDN3 [NCBI] 8.98963e-05
EDNRB [NCBI] 5.55109e-05
TYRP1 [NCBI] 1.98771e-05
GJB2 [NCBI] 1.79105e-05
TFE3 [NCBI] 1.38741e-05
TYR [NCBI] 1.23304e-05
ONECUT2 [NCBI] 1.15825e-05
SNAI2 [NCBI] 9.83163e-06
SOX11 [NCBI] 9.28141e-06
CHRND [NCBI] 8.95368e-06
POU3F1 [NCBI] 8.95368e-06
ALPI [NCBI] 8.81071e-06
CLRN1 [NCBI] 8.13905e-06
PAX1 [NCBI] 7.72966e-06
PAX4 [NCBI] 6.97738e-06
UBE2I [NCBI] 6.56454e-06
PAX9 [NCBI] 6.39066e-06
PAX7 [NCBI] 6.2032e-06
OCA2 [NCBI] 5.7635e-06
GJB6 [NCBI] 5.49118e-06
FN1 [NCBI] 5.27407e-06
PAX2 [NCBI] 4.93762e-06
PAX8 [NCBI] 4.83051e-06
GSK3B [NCBI] 4.79208e-06
PAX5 [NCBI] 4.70577e-06
SOX9 [NCBI] 4.65841e-06
DCT [NCBI] 4.01264e-06
PAX6 [NCBI] 3.44152e-06
SLC6A4 [NCBI] 2.17978e-06




OMIM


OMIM Link Information
gain
01
WS1 [NCBI] 0.00571134
microphthalmia with limb anomalies [NCBI] 0.0034825
WS2B [NCBI] 0.003153
PAX3 [NCBI] 0.00298892
ADFN [NCBI] 0.00214098
MITF [NCBI] 0.00137362
WS2A [NCBI] 0.00126209
waardenburg-shah syndrome [NCBI] 0.00104624
waardenburg syndrome, type iic [NCBI] 0.0010375
WS3 [NCBI] 0.000904373
deafness, congenital, with vitiligo and achalasia [NCBI] 0.000819746
SOX10 [NCBI] 0.000570429
acrodysostosis [NCBI] 0.000545541
EDN3 [NCBI] 0.00045542
tietz syndrome [NCBI] 0.000408107
albinism, ocular, with sensorineural deafness [NCBI] 0.00033621
PCWH [NCBI] 0.000299763
HSCR1 [NCBI] 0.000276739
CDHS [NCBI] 0.000179044
EDNRB [NCBI] 0.000176727
ALPI [NCBI] 0.000146616
WS2E [NCBI] 0.000111888
waardenburg syndrome, type iid [NCBI] 8.94311e-05
abcd syndrome [NCBI] 8.09651e-05
TYR [NCBI] 5.73282e-05
PBT [NCBI] 5.49323e-05
PAX4 [NCBI] 5.42838e-05
PAX7 [NCBI] 5.42838e-05
UBE2I [NCBI] 5.42838e-05
HPS [NCBI] 5.33556e-05
SNAI2 [NCBI] 5.09122e-05
CHRND [NCBI] 4.84067e-05
crouzon syndrome [NCBI] 4.78347e-05
CHS [NCBI] 4.54257e-05
dyschromatosis symmetrica hereditaria 1 [NCBI] 4.23908e-05
PAX1 [NCBI] 4.20947e-05
PAX9 [NCBI] 4.09941e-05
PAX5 [NCBI] 3.91059e-05
ODDD [NCBI] 3.8381e-05
PAX8 [NCBI] 3.68192e-05
OCA1A [NCBI] 3.55769e-05
FN1 [NCBI] 3.49679e-05
TCOF1 [NCBI] 3.29461e-05
PAX2 [NCBI] 3.25003e-05
TCOF [NCBI] 2.87088e-05
HGPS [NCBI] 2.67972e-05
ASS [NCBI] 2.15815e-05
GDNF [NCBI] 1.95156e-05
BCNS [NCBI] 1.51349e-05
dystrophia myotonica 1 [NCBI] 1.10086e-05
HD [NCBI] 2.94552e-06




Database Center for Life Science