Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Sweat [NCBI]

Gene


 Gene Link Information
Gain		 01
CFTR [NCBI] 0.000632328
DCD [NCBI] 4.25346e-05
PRSS1 [NCBI] 1.06034e-05
CAMP [NCBI] 9.12372e-06
GPR182 [NCBI] 5.71563e-06
CST6 [NCBI] 5.00428e-06
PRSS2 [NCBI] 4.77782e-06
SPINK1 [NCBI] 4.56971e-06
ATP7B [NCBI] 4.41766e-06
CTSD [NCBI] 3.67441e-06
PIP [NCBI] 3.61905e-06
PRL [NCBI] 3.55243e-06
AVP [NCBI] 2.50075e-06
IL1RN [NCBI] 1.37405e-06
AFP [NCBI] 1.19835e-06
VIP [NCBI] 5.45442e-07
PTH [NCBI] 3.99395e-07



OMIM


 OMIM Link Information
gain		 01
CF [NCBI] 0.00907294
mucus inspissation of respiratory tract [NCBI] 0.00137599
kohlschutter-tonz syndrome [NCBI] 0.00108094
microcephaly, hiatus hernia, and nephrotic syndrome [NCBI] 0.00104348
CFTR [NCBI] 0.000848554
thrombocytopenia-absent radius syndrome [NCBI] 0.0007219
RA [NCBI] 0.00056461
DCD [NCBI] 0.000260068
PHA1 [NCBI] 0.000179579
histidinemia [NCBI] 0.000174251
anhidrosis [NCBI] 0.000163187
spondyloepimetaphyseal dysplasia with hypotrichosis [NCBI] 0.000163187
emphysema, hereditary pulmonary [NCBI] 0.000163187
PCTT [NCBI] 0.000131133
tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities [NCBI] 0.000123999
glycinuria with or without oxalate urolithiasis [NCBI] 0.000109263
TMAU [NCBI] 8.70399e-05
halothane hepatitis [NCBI] 7.84127e-05
methionine adenosyltransferase deficiency [NCBI] 6.43721e-05
CIPA [NCBI] 6.43721e-05
GCE [NCBI] 6.22797e-05
CBAVD [NCBI] 5.23929e-05
HYPP [NCBI] 4.74623e-05
PFIC1 [NCBI] 4.63707e-05
CST6 [NCBI] 4.11215e-05
CTNS [NCBI] 3.61458e-05
ED1 [NCBI] 3.01774e-05
SPINK1 [NCBI] 2.11554e-05
PRL [NCBI] 1.04156e-05
AVP [NCBI] 5.85145e-06
AFP [NCBI] 3.57487e-06
NPPA [NCBI] 3.10219e-06
VIP [NCBI] 4.22817e-07
PTH [NCBI] 8.99786e-08
ALD [NCBI] 2.63423e-09



Database Center for Life Science