EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.7.7.80 | Encephalomalacia |
33897766 |
Case Report: Compound Heterozygous Variants in MOCS3 Identified in a Chinese Infant With Molybdenum Cofactor Deficiency. |
causal interaction
unassigned |
3
0 |
| 2.7.7.80 | Neurologic Manifestations |
33897766 |
Case Report: Compound Heterozygous Variants in MOCS3 Identified in a Chinese Infant With Molybdenum Cofactor Deficiency. |
causal interaction
unassigned |
3
0 |
| 2.7.7.80 | Perinatal Death |
33897766 |
Case Report: Compound Heterozygous Variants in MOCS3 Identified in a Chinese Infant With Molybdenum Cofactor Deficiency. |
causal interaction
unassigned |
3
0 |
| 2.7.7.80 | Pulmonary Disease, Chronic Obstructive |
26917578 |
Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
2
3
1
0 |
