MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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