EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    3.2.1.22 | Abortion, Spontaneous |
15248154 |
Trisomy recurrence: a reconsideration based on North American data. |
therapeutic application
unassigned |
1
0 |
| 3.2.1.22 | Adenocarcinoma |
4049371 |
Alteration in glycosidases from well-differentiated colorectal adenocarcinoma of rat. |
diagnostic usage
unassigned |
4
0 |
| 3.2.1.22 | AIDS-Associated Nephropathy |
8840936 |
Molecular therapy for renal diseases. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
3
2
3
0 |
| 3.2.1.22 | alpha-galactosidase deficiency |
417009 |
[Clinical, preclinical and prenatal diagnosis of congenital sphingolipidoses by determining lysosomal hydrolases (author's transl)] |
causal interaction
diagnostic usage
unassigned |
4
4
0 |
| 3.2.1.22 | alpha-galactosidase deficiency |
2890570 |
Anderson Fabry disease, a close linkage with highly polymorphic DNA markers DXS17, DXS87 and DXS88. |
causal interaction
unassigned |
4
0 |
| 3.2.1.22 | alpha-galactosidase deficiency |
2908672 |
Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes. |
causal interaction
unassigned |
4
0 |
| 3.2.1.22 | alpha-galactosidase deficiency |
2999674 |
Corneal alpha-galactosidase deficiency in macular corneal dystrophy. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
4
4
0 |
| 3.2.1.22 | alpha-galactosidase deficiency |
3035532 |
Prenatal diagnosis of Fabry's disease by direct analysis of chorionic villi. |
causal interaction
unassigned |
2
0 |
| 3.2.1.22 | alpha-galactosidase deficiency |
4212108 |
Investigation of the alpha-galactosidase deficiency in Fabry's disease using antibodies against the purified enzyme. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
| 3.2.1.22 | alpha-galactosidase deficiency |
5411915 |
Fabry's disease: alpha-galactosidase deficiency. |
causal interaction
unassigned |
4
0 |
