Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Umbilicus [NCBI]

Gene


 Gene Link Information
Gain		 01
PITX3 [NCBI] 2.32962e-05
PITX1 [NCBI] 2.23934e-05
SERPINF2 [NCBI] 8.1639e-06
PITX2 [NCBI] 7.54735e-06
IFNG [NCBI] 5.30614e-06
PAX6 [NCBI] 4.5655e-06
TGFB1 [NCBI] 3.52559e-06
EGF [NCBI] 2.1258e-06



OMIM


 OMIM Link Information
gain		 01
umbilicus, familial flat [NCBI] 0.00163019
mesomelia-synostoses syndrome [NCBI] 0.00131934
RIEG2 [NCBI] 0.00112601
RIEG1 [NCBI] 0.00100971
robinow syndrome, autosomal dominant [NCBI] 0.000779239
FSHMD1A [NCBI] 0.00043266
faciogenital dysplasia [NCBI] 0.000258642
BWS [NCBI] 0.000256848
aortic aneurysm, giant congenital [NCBI] 0.000177222
PXE [NCBI] 0.000168243
hemangiomas, cavernous, of face and supraumbilical midline raphe [NCBI] 0.000160451
IRID2 [NCBI] 0.000136444
LAD [NCBI] 9.64198e-05
plasmin inhibitor deficiency [NCBI] 5.55083e-05
PITX2 [NCBI] 4.71073e-05
ITGB2 [NCBI] 4.30625e-05
EGF [NCBI] 6.43453e-06



Database Center for Life Science