Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Fistula [NCBI]

Gene


 Gene Link Information
Gain		 01
CCK [NCBI] 3.33691e-05
PYY [NCBI] 3.17002e-05
POU3F4 [NCBI] 1.25702e-05
BMI1 [NCBI] 9.53225e-06
MMP1 [NCBI] 8.17706e-06
BAK1 [NCBI] 8.1171e-06
GIP [NCBI] 8.09112e-06
CLU [NCBI] 7.80673e-06
MMP2 [NCBI] 7.21371e-06
MMP9 [NCBI] 6.82934e-06
NPY [NCBI] 5.06871e-06



OMIM


 OMIM Link Information
gain		 01
preauricular fistulae, congenital [NCBI] 0.00098052
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging [NCBI] 0.000632907
chiari malformation type i [NCBI] 0.000533713
palatopharyngeal incompetence [NCBI] 0.000473897
BOR1 [NCBI] 0.000372681
HFM [NCBI] 0.00035865
VWS [NCBI] 0.000327765
CCK [NCBI] 0.000156792
PYY [NCBI] 0.000155665
AVSD [NCBI] 0.000128321
BOS1 [NCBI] 7.97164e-05
waardenburg-shah syndrome [NCBI] 7.77539e-05
EVA [NCBI] 6.63352e-05
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 6.50282e-05
CES [NCBI] 6.03475e-05
CPI [NCBI] 3.85656e-05
GIP [NCBI] 3.60309e-05
TS [NCBI] 2.38534e-05
NPY [NCBI] 1.87273e-05
SLE [NCBI] 4.85239e-06



Database Center for Life Science