| MeSH_gene2pubmed |
B_14_38 |
D012857 |
Situs Inversus |
2/16 |
29/26076 |
0.00014193017618014 |
0.0244119903029848 |
0.0178533221616076 |
INVS/NPHP3 |
2 |
| MeSH_gene2pubmed |
B_14_38 |
D017044 |
Polycystic Kidney, Autosomal Recessive |
2/16 |
29/26076 |
0.00014193017618014 |
0.0244119903029848 |
0.0178533221616076 |
INVS/NPHP3 |
2 |
| MeSH_gene2pubmed |
B_14_38 |
D001656 |
Biliary Atresia |
2/16 |
56/26076 |
0.00053318021028754 |
0.0449470514251108 |
0.0328713136187316 |
ATP8B1/INVS |
2 |
| MeSH_gene2pubmed |
B_14_38 |
D001629 |
Bezafibrate |
2/16 |
57/26076 |
0.00055237095963202 |
0.0449470514251108 |
0.0328713136187316 |
ATP8B1/PPARD |
2 |
| MeSH_gene2pubmed |
B_14_38 |
D052177 |
Kidney Diseases, Cystic |
2/16 |
62/26076 |
0.00065330016606265 |
0.0449470514251108 |
0.0328713136187316 |
INVS/NPHP3 |
2 |
| WikiPathways |
B_14_38 |
WP4577 |
Neurodegeneration with brain iron accumulation NBIA subtypes pathway |
2/8 |
44/8836 |
0.0006658112167592 |
0.0213059589362945 |
0.0112136625980497 |
ATG10/DCAF17 |
2 |
| WikiPathways |
B_14_38 |
WP4656 |
Joubert syndrome |
2/8 |
76/8836 |
0.00197697242886009 |
0.0281702629309516 |
0.0148264541741851 |
INVS/NPHP3 |
2 |
| WikiPathways |
B_14_38 |
WP5234 |
Bardet Biedl syndrome |
2/8 |
88/8836 |
0.00264096214977672 |
0.0281702629309516 |
0.0148264541741851 |
INVS/NPHP3 |
2 |
| hallmark |
B_14_38 |
HALLMARK_NOTCH_SIGNALING |
HALLMARK_NOTCH_SIGNALING |
1/3 |
32/4384 |
0.0217432852408486 |
0.0496917328044446 |
0.0209228348650293 |
PPARD |
1 |
| hallmark |
B_14_38 |
HALLMARK_WNT_BETA_CATENIN_SIGNALING |
HALLMARK_WNT_BETA_CATENIN_SIGNALING |
1/3 |
42/4384 |
0.0284728425087264 |
0.0496917328044446 |
0.0209228348650293 |
PPARD |
1 |