EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.8.2.17 | Adenocarcinoma |
11056388 |
Molecular cloning, expression, and chromosomal mapping of human chondroitin 4-sulfotransferase, whose expression pattern in human tissues is different from that of chondroitin 6-sulfotransferase. |
causal interaction
unassigned |
4
0 |
| 2.8.2.17 | Atherosclerosis |
9639683 |
Human chondroitin 6-sulfotransferase: cloning, gene structure, and chromosomal localization. |
unassigned |
0 |
| 2.8.2.17 | Brain Injuries |
15673437 |
Chondroitin 6-sulphate synthesis is up-regulated in injured CNS, induced by injury-related cytokines and enhanced in axon-growth inhibitory glia. |
unassigned |
0 |
| 2.8.2.17 | chondroitin 6-sulfotransferase deficiency |
18513679 |
Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis. |
causal interaction
unassigned |
3
0 |
| 2.8.2.17 | chondroitin 6-sulfotransferase deficiency |
20830804 |
Phenotypic features of carbohydrate sulfotransferase 3 (CHST3) deficiency in 24 patients: congenital dislocations and vertebral changes as principal diagnostic features. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.8.2.17 | Clubfoot |
26572954 |
A novel CHST3 allele associated with Spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred. |
causal interaction
unassigned |
4
0 |
| 2.8.2.17 | Contracture |
26572954 |
A novel CHST3 allele associated with Spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred. |
causal interaction
unassigned |
4
0 |
| 2.8.2.17 | Contracture |
32639237 |
Recurrent c.776T>C mutation in CHST3 with four other novel mutations and a literature review. |
causal interaction
unassigned |
4
0 |
| 2.8.2.17 | Deafness |
18698629 |
Spondyloepiphyseal dysplasia, Omani type: further definition of the phenotype. |
unassigned |
0 |
| 2.8.2.17 | Dysostoses |
18513679 |
Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis. |
causal interaction
unassigned |
3
0 |
