Pages that link to "Property:P409"
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The following pages link to exact match (P409):
Displaying 50 items.
- oxidoreductase activity, acting on X-H and Y-H to form an X-Y bond (Q16206) (← links)
- oligohydramnios (Q16207) (← links)
- isopenicillin-N epimerase activity (Q16211) (← links)
- deacetoxycephalosporin-C synthase activity (Q16213) (← links)
- oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, with 2-oxoglutarate as one donor, and the other dehydrogenated (Q16214) (← links)
- obstetric labor complication (Q16216) (← links)
- deacetoxycephalosporin-C hydroxylase activity (Q16218) (← links)
- deacetylcephalosporin-C acetyltransferase activity (Q16220) (← links)
- C-acyltransferase activity (Q16221) (← links)
- large for gestational age (Q16223) (← links)
- cephalosporin-C deacetylase activity (Q16225) (← links)
- deacetylase activity (Q16226) (← links)
- cephalosporin-C transaminase activity (Q16228) (← links)
- cephalosporin C metabolic process (Q16231) (← links)
- cephalosporin metabolic process (Q16232) (← links)
- beta-lactam antibiotic metabolic process (Q16233) (← links)
- cellular lactam metabolic process (Q16234) (← links)
- infant respiratory distress syndrome (Q16235) (← links)
- antibiotic metabolic process (Q16237) (← links)
- congenital diaphragmatic hernia (Q16238) (← links)
- diaphragm disease (Q16239) (← links)
- cephalosporin C catabolic process (Q16246) (← links)
- beta-lactam antibiotic catabolic process (Q16247) (← links)
- cellular lactam catabolic process (Q16248) (← links)
- antibiotic catabolic process (Q16249) (← links)
- cephalosporin C biosynthetic process (Q16250) (← links)
- cephalosporin biosynthetic process (Q16251) (← links)
- beta-lactam antibiotic biosynthetic process (Q16252) (← links)
- cellular lactam biosynthetic process (Q16253) (← links)
- antibiotic biosynthetic process (Q16256) (← links)
- hernia (Q16259) (← links)
- rare genetic developmental defect during embryogenesis (Q16261) (← links)
- rare genetic respiratory disease (Q16262) (← links)
- congenital heart disease (Q16263) (← links)
- genetic cardiac disease (Q16265) (← links)
- rare cardiac disease (Q16266) (← links)
- rare circulatory system disease (Q16267) (← links)
- hypoxemia (Q16268) (← links)
- cerebral palsy (Q16276) (← links)
- cerebral degeneration (Q16277) (← links)
- paralysis (Q16279) (← links)
- tic (Q16280) (← links)
- tic disorder (Q16281) (← links)
- gait abnormality (Q16285) (← links)
- movement disorders (Q16286) (← links)
- isopenicillin-N N-acyltransferase activity (Q16288) (← links)
- cysteine lyase activity (Q16292) (← links)
- glutathione-cystine transhydrogenase activity (Q16294) (← links)
- molybdenum cofactor sulfurtransferase activity (Q16296) (← links)
- sulfurtransferase activity (Q16297) (← links)