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 |