Skip navigation

Pathways Pathways

1–100 of 145 'D' pathways.
1. Has associated genes. Has associated diseases. DAG and IP3 signaling REACT:R-HSA-1489509
2. Has associated genes. Has associated diseases. DAP12 interactions REACT:R-HSA-2172127
3. Has associated genes. Has associated diseases. DAP12 signaling REACT:R-HSA-2424491
4. Has associated genes. Has associated diseases. D-Arginine and D-ornithine metabolism KEGG:hsa00472
5. Has associated genes. Has associated diseases. DARPP-32 events REACT:R-HSA-180024
6. Has associated genes. Has associated diseases. DCC mediated attractive signaling REACT:R-HSA-418885
7. Has associated genes. Has associated diseases. Deactivation of the beta-catenin transactivating complex REACT:R-HSA-3769402
8. Has associated genes. Has associated diseases. Deadenylation-dependent mRNA decay REACT:R-HSA-429914
9. Has associated genes. Has associated diseases. Deadenylation of mRNA REACT:R-HSA-429947
10. Has associated genes. Has associated diseases. Death Receptor Signalling REACT:R-HSA-73887
11. Has associated genes. Has associated diseases. Decapping complex KEGG:hsa_M00395
12. Has associated genes. Has associated diseases. Dectin-1 mediated noncanonical NF-kB signaling REACT:R-HSA-5607761
13. Has associated genes. Has associated diseases. Dectin-2 family REACT:R-HSA-5621480
14. Has associated genes. Has associated diseases. Defective ABCA3 causes pulmonary surfactant metabolism dysfunction type 3 (SMDP3) REACT:R-HSA-5683678
15. Has associated genes. Has associated diseases. Defective ABCC8 can cause hypoglycemias and hyperglycemias REACT:R-HSA-5683177
16. Has associated genes. Has associated diseases. Defective ACTH causes Obesity and Pro-opiomelanocortinin deficiency (POMCD) REACT:R-HSA-5579031
17. Has associated genes. Has associated diseases. Defective AMN causes hereditary megaloblastic anemia 1 REACT:R-HSA-3359462
18. Has associated genes. Has associated diseases. Defective AVP causes neurohypophyseal diabetes insipidus (NDI) REACT:R-HSA-5619099
19. Has associated genes. Has associated diseases. Defective B3GALT6 causes EDSP2 and SEMDJL1 REACT:R-HSA-4420332
20. Has associated genes. Has associated diseases. Defective B3GALTL causes Peters-plus syndrome (PpS) REACT:R-HSA-5083635
21. Has associated genes. Has associated diseases. Defective B3GAT3 causes JDSSDHD REACT:R-HSA-3560801
22. Has associated genes. Has associated diseases. Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) REACT:R-HSA-3656244
23. Has associated genes. Has associated diseases. Defective B4GALT7 causes EDS, progeroid type REACT:R-HSA-3560783
24. Has associated genes. Has associated diseases. Defective C1GALT1C1 causes Tn polyagglutination syndrome (TNPS) REACT:R-HSA-5083632
25. Has associated genes. Has associated diseases. Defective CD320 causes methylmalonic aciduria REACT:R-HSA-3359485
26. Has associated genes. Has associated diseases. Defective CFTR causes cystic fibrosis REACT:R-HSA-5678895
27. Has associated genes. Has associated diseases. Defective CHST14 causes EDS, musculocontractural type REACT:R-HSA-3595174
28. Has associated genes. Has associated diseases. Defective CHST3 causes SEDCJD REACT:R-HSA-3595172
29. Has associated genes. Has associated diseases. Defective CHST6 causes MCDC1 REACT:R-HSA-3656225
30. Has associated genes. Has associated diseases. Defective CHSY1 causes TPBS REACT:R-HSA-3595177
31. Has associated genes. Has associated diseases. Defective CSF2RA causes pulmonary surfactant metabolism dysfunction 4 (SMDP4) REACT:R-HSA-5688890
32. Has associated genes. Has associated diseases. Defective CSF2RB causes pulmonary surfactant metabolism dysfunction 5 (SMDP5) REACT:R-HSA-5688849
33. Has associated genes. Has associated diseases. Defective CUBN causes hereditary megaloblastic anemia 1 REACT:R-HSA-3359463
34. Has associated genes. Has associated diseases. Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR) REACT:R-HSA-5579026
35. Has associated genes. Has associated diseases. Defective EXT1 causes exostoses 1, TRPS2 and CHDS REACT:R-HSA-3656253
36. Has associated genes. Has associated diseases. Defective EXT2 causes exostoses 2 REACT:R-HSA-3656237
37. Has associated genes. Has associated diseases. Defective GALNT12 causes colorectal cancer 1 (CRCS1) REACT:R-HSA-5083636
38. Has associated genes. Has associated diseases. Defective GALNT3 causes familial hyperphosphatemic tumoral calcinosis (HFTC) REACT:R-HSA-5083625
39. Has associated genes. Has associated diseases. Defective GIF causes intrinsic factor deficiency REACT:R-HSA-3359457
40. Has associated genes. Has associated diseases. Defective HLCS causes multiple carboxylase deficiency REACT:R-HSA-3371599
41. Has associated genes. Has associated diseases. Defective LFNG causes SCDO3 REACT:R-HSA-5083630
42. Has associated genes. Has associated diseases. Defective MMAA causes methylmalonic aciduria type cblA REACT:R-HSA-3359475
43. Has associated genes. Has associated diseases. Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC REACT:R-HSA-3359474
44. Has associated genes. Has associated diseases. Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD REACT:R-HSA-3359473
45. Has associated genes. Has associated diseases. Defective MTR causes methylmalonic aciduria and homocystinuria type cblG REACT:R-HSA-3359469
46. Has associated genes. Has associated diseases. Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE REACT:R-HSA-3359467
47. Has associated genes. Has associated diseases. Defective MUT causes methylmalonic aciduria mut type REACT:R-HSA-3359478
48. Has associated genes. Has associated diseases. Defective POMGNT1 causes MDDGA3, MDDGB3 and MDDGC3 REACT:R-HSA-5083628
49. Has associated genes. Has associated diseases. Defective POMT1 causes MDDGA1, MDDGB1 and MDDGC1 REACT:R-HSA-5083633
50. Has associated genes. Has associated diseases. Defective POMT2 causes MDDGA2, MDDGB2 and MDDGC2 REACT:R-HSA-5083629
51. Has associated genes. Has associated diseases. Defective pro-SFTPB causes pulmonary surfactant metabolism dysfunction 1 (SMDP1) and respiratory distress syndrome (RDS) REACT:R-HSA-5688031
52. Has associated genes. Has associated diseases. Defective pro-SFTPC causes pulmonary surfactant metabolism dysfunction 2 (SMDP2) and respiratory distress syndrome (RDS) REACT:R-HSA-5688354
53. Has associated genes. Has associated diseases. Defective SFTPA2 causes idiopathic pulmonary fibrosis (IPF) REACT:R-HSA-5687868
54. Has associated genes. Has associated diseases. Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR) REACT:R-HSA-5619110
55. Has associated genes. Has associated diseases. Defective SLCO1B3 causes hyperbilirubinemia, Rotor type (HBLRR) REACT:R-HSA-5619058
56. Has associated genes. Has associated diseases. Defective ST3GAL3 causes MCT12 and EIEE15 REACT:R-HSA-3656243
57. Has associated genes. Has associated diseases. Defective TCN2 causes hereditary megaloblastic anemia REACT:R-HSA-3359454
58. Has associated genes. Has associated diseases. Defective TRP may confer susceptibility towards thyroid papillary carcinoma (TPC) REACT:R-HSA-5619107
59. Has associated genes. Has associated diseases. Defects in biotin (Btn) metabolism REACT:R-HSA-3323169
60. Has associated genes. Has associated diseases. Defects in cobalamin (B12) metabolism REACT:R-HSA-3296469
61. Has associated genes. Has associated diseases. Defects in vitamin and cofactor metabolism REACT:R-HSA-3296482
62. Has associated genes. Has associated diseases. Defensins REACT:R-HSA-1461973
63. Has associated genes. Has associated diseases. Degradation of AXIN REACT:R-HSA-4641257
64. Has associated genes. Has associated diseases. Degradation of beta-catenin by the destruction complex REACT:R-HSA-195253
65. Has associated genes. Has associated diseases. Degradation of cysteine and homocysteine REACT:R-HSA-1614558
66. Has associated genes. Has associated diseases. Degradation of DVL REACT:R-HSA-4641258
67. Has associated genes. Has associated diseases. Degradation of GABA REACT:R-HSA-916853
68. Has associated genes. Has associated diseases. Degradation of GLI1 by the proteasome REACT:R-HSA-5610780
69. Has associated genes. Has associated diseases. Degradation of GLI2 by the proteasome REACT:R-HSA-5610783
70. Has associated genes. Has associated diseases. Degradation of the extracellular matrix REACT:R-HSA-1474228
71. Has associated genes. Has associated diseases. Depolarization of the Presynaptic Terminal Triggers the Opening of Calcium Channels REACT:R-HSA-112308
72. Has associated genes. Has associated diseases. Depolymerisation of the Nuclear Lamina REACT:R-HSA-4419969
73. Has associated genes. Has associated diseases. Deposition of new CENPA-containing nucleosomes at the centromere REACT:R-HSA-606279
74. Has associated genes. Has associated diseases. Depurination REACT:R-HSA-73927
75. Has associated genes. Has associated diseases. Depyrimidination REACT:R-HSA-73928
76. Has associated genes. Has associated diseases. Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models REACT:R-HSA-8862803
77. Has associated genes. Has associated diseases. Dermatan sulfate biosynthesis REACT:R-HSA-2022923
78. Has associated genes. Has associated diseases. Dermatan sulfate degradation KEGG:hsa_M00076
79. Has associated genes. Has associated diseases. Detoxification of Reactive Oxygen Species REACT:R-HSA-3299685
80. Has associated genes. Has associated diseases. Deubiquitination REACT:R-HSA-5688426
81. Has associated genes. Has associated diseases. Developmental Biology REACT:R-HSA-1266738
82. Has associated genes. Has associated diseases. DEx/H-box helicases activate type I IFN and inflammatory cytokines production REACT:R-HSA-3134963
83. Has associated genes. Has associated diseases. D-Glutamine and D-glutamate metabolism KEGG:hsa00471
84. Has associated genes. Has associated diseases. Digestion of dietary carbohydrate REACT:R-HSA-189085
85. Has associated genes. Has associated diseases. Digestion of dietary lipid REACT:R-HSA-192456
86. Has associated genes. Has associated diseases. Dilated cardiomyopathy KEGG:hsa05414
87. Has associated genes. Has associated diseases. Dimerization of procaspase-8 REACT:R-HSA-69416
88. Has associated genes. Has associated diseases. Disassembly of the destruction complex and recruitment of AXIN to the membrane REACT:R-HSA-4641262
89. Has associated genes. Has associated diseases. Disease REACT:R-HSA-1643685
90. Has associated genes. Has associated diseases. Diseases associated with glycosaminoglycan metabolism REACT:R-HSA-3560782
91. Has associated genes. Has associated diseases. Diseases associated with O-glycosylation of proteins REACT:R-HSA-3906995
92. Has associated genes. Has associated diseases. Diseases associated with surfactant metabolism REACT:R-HSA-5687613
93. Has associated genes. Has associated diseases. Diseases associated with the TLR signaling cascade REACT:R-HSA-5602358
94. Has associated genes. Has associated diseases. Diseases associated with visual transduction REACT:R-HSA-2474795
95. Has associated genes. Has associated diseases. Diseases of carbohydrate metabolism REACT:R-HSA-5663084
96. Has associated genes. Has associated diseases. Diseases of glycosylation REACT:R-HSA-3781865
97. Has associated genes. Has associated diseases. Diseases of Immune System REACT:R-HSA-5260271
98. Has associated genes. Has associated diseases. Diseases of metabolism REACT:R-HSA-5668914
99. Has associated genes. Has associated diseases. Diseases of signal transduction REACT:R-HSA-5663202
100. Has associated genes. Has associated diseases. Disinhibition of SNARE formation REACT:R-HSA-114516
1–100 of 145 'D' pathways.