Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Piebaldism [NCBI]

Gene


 Gene Link Information
Gain		 01
KIT [NCBI] 0.000152788
RAB27A [NCBI] 6.24988e-05
MYO5A [NCBI] 2.45956e-05
DCT [NCBI] 1.65114e-05
SNAI2 [NCBI] 1.59721e-05
EDN3 [NCBI] 1.04639e-05
OCA2 [NCBI] 8.81607e-06
MITF [NCBI] 7.09685e-06
PAX3 [NCBI] 6.8549e-06
CXCL1 [NCBI] 6.47242e-06
SLC6A4 [NCBI] 5.0849e-06



OMIM


 OMIM Link Information
gain		 01
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging [NCBI] 0.00102539
KIT [NCBI] 0.000669687
PBT [NCBI] 0.000483625
HPS [NCBI] 0.000129303
piebald trait with neurologic defects [NCBI] 0.000127588
CHS [NCBI] 0.000120678
GS2 [NCBI] 9.4278e-05
dyschromatosis symmetrica hereditaria 1 [NCBI] 8.0164e-05
RAB27A [NCBI] 5.72439e-05
DBA [NCBI] 5.62157e-05
EDN3 [NCBI] 5.35922e-05
KITLG [NCBI] 4.22076e-05
MITF [NCBI] 3.96704e-05



Database Center for Life Science