EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    5.4.2.8 | Acquired Immunodeficiency Syndrome |
31600460 |
Meeting the Best Practice for Hearing Aid Verification in Children: Challenges and Future Directions. |
causal interaction
therapeutic application
unassigned |
1
3
0 |
| 5.4.2.8 | adenosylhomocysteinase deficiency |
22959829 |
Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency. |
causal interaction
unassigned |
3
0 |
| 5.4.2.8 | Aggressive Periodontitis |
9028263 |
Development and evaluation of a selective and differential medium for the primary isolation of Peptostreptococcus micros. |
causal interaction
diagnostic usage
ongoing research
unassigned |
1
3
2
0 |
| 5.4.2.8 | Agranulocytosis |
8656680 |
Prednimustine, mitoxantrone (PmM) vs cyclophosphamide, vincristine, prednisone (COP) for the treatment of advanced low-grade non-Hodgkin's lymphoma. German Low-Grade Lymphoma Study Group. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
3
2
2
0 |
| 5.4.2.8 | Alopecia |
6781747 |
Phase I trial of pentamethylmelamine in patients with previously treated malignancies. |
ongoing research
unassigned |
3
0 |
| 5.4.2.8 | alpha-1,6-mannosyl-glycoprotein 2-beta-n-acetylglucosaminyltransferase deficiency |
9455908 |
Hypoglycosylation of a brain glycoprotein (beta-trace protein) in CDG syndromes due to phosphomannomutase deficiency and N-acetylglucosaminyl-transferase II deficiency. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
2
1
0 |
| 5.4.2.8 | Arthritis |
28184957 |
Partial meniscectomy provides no benefit for symptomatic degenerative medial meniscus posterior root tears. |
causal interaction
diagnostic usage
unassigned |
1
1
0 |
| 5.4.2.8 | Astrocytoma |
6432969 |
Human central nervous system pharmacology of pentamethylmelamine and its metabolites. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
3
2
1
3 |
| 5.4.2.8 | Ataxia |
17694350 |
Cerebellar ataxia and congenital disorder of glycosylation Ia (CDG-Ia) with normal routine CDG screening. |
diagnostic usage
unassigned |
3
0 |
| 5.4.2.8 | Ataxia |
26502900 |
Phosphomannomutase deficiency (PMM2-CDG): ataxia and cerebellar assessment. |
causal interaction
unassigned |
4
0 |
