EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.4.1.142 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
14973778 |
Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik. |
causal interaction
unassigned |
4
0 |
| 2.4.1.142 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
14973782 |
Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I. |
unassigned |
0 |
| 2.4.1.142 | Pemphigoid, Bullous |
23252972 |
A successful treatment with ustekunumab in a case of anti-laminin-?1 pemphigoid associated with psoriasis. |
causal interaction
therapeutic application
unassigned |
3
1
0 |
| 2.4.1.142 | Psoriasis |
23252972 |
A successful treatment with ustekunumab in a case of anti-laminin-?1 pemphigoid associated with psoriasis. |
causal interaction
therapeutic application
unassigned |
3
1
0 |
