EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.7.1.108 | Carcinoma, Hepatocellular |
2836054 |
Cytidine 5'-triphosphate-dependent dolichol kinase and dolichol phosphatase activities and levels of dolichyl phosphate in microsomal fractions from highly differentiated human hepatomas. |
diagnostic usage
ongoing research
unassigned |
3
4
0 |
| 2.7.1.108 | Cardiomyopathy, Dilated |
22327749 |
From discrete dilated cardiomyopathy to successful cardiac transplantation in congenital disorders of glycosylation due to dolichol kinase deficiency (DK1-CDG). |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.7.1.108 | Congenital Disorders of Glycosylation |
22327749 |
From discrete dilated cardiomyopathy to successful cardiac transplantation in congenital disorders of glycosylation due to dolichol kinase deficiency (DK1-CDG). |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.7.1.108 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
22327749 |
From discrete dilated cardiomyopathy to successful cardiac transplantation in congenital disorders of glycosylation due to dolichol kinase deficiency (DK1-CDG). |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.7.1.108 | Cysts |
2553851 |
Dolichol phosphorylation occurs via a CTP-dependent reaction in Artemia larvae. |
ongoing research
unassigned |
2
0 |
| 2.7.1.108 | dolichol kinase deficiency |
22242004 |
Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation. |
causal interaction
diagnostic usage
unassigned |
4
3
0 |
| 2.7.1.108 | dolichol kinase deficiency |
22327749 |
From discrete dilated cardiomyopathy to successful cardiac transplantation in congenital disorders of glycosylation due to dolichol kinase deficiency (DK1-CDG). |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.7.1.108 | dolichol kinase deficiency |
23890587 |
Dolichol kinase deficiency (DOLK-CDG) with a purely neurological presentation caused by a novel mutation. |
causal interaction
unassigned |
4
0 |
| 2.7.1.108 | dolichol kinase deficiency |
28816422 |
Dolichol kinase deficiency (DOLK-CDG): Two new cases and expansion of phenotype. |
causal interaction
diagnostic usage
unassigned |
4
3
0 |
| 2.7.1.108 | dolichol kinase deficiency |
32250540 |
Fatal hyperkeratosis syndrome in four siblings due to dolichol kinase deficiency. |
causal interaction
unassigned |
3
0 |
