Experimental Factor Ontology
3040 terms(s) returned
| Term Type: | Record: 2501 to 2550 of 3040 Records | Page: 51 of 61, First Previous Next Last | Show Records Per Page |
- glycodeoxycholate
- glycodeoxycholate 3-O-glucuronide measurement
- glycodeoxycholate 3-sulfate measurement
- glycodeoxycholate measurement
- glycogen [starch] synthase, muscle
- glycogen [starch] synthase, muscle (human)
- glycogen metabolic process
- glycogen phosphorylase, brain form
- glycogen phosphorylase, brain form (human)
- glycogen phosphorylase, brain form, initiator methionine removed form
- glycogen phosphorylase, liver form
- glycogen phosphorylase, liver form (human)
- glycogen phosphorylase, liver form measurement
- glycogen phosphorylase, liver form, initiator methionine removed form
- glycogen storage disease I
- glycogen storage disease II
- glycogen storage disease III
- glycogen storage disease IX
- glycogen storage disease IXa1
- glycogen storage disease IXb
- glycogen storage disease IXc
- glycogen storage disease IXd
- glycogen storage disease Ib
- glycogen storage disease V
- glycogen storage disease VI
- glycogen storage disease VII
- glycogen storage disease VIII
- glycogen storage disease XV
- glycogen storage disease due to GLUT2 deficiency
- glycogen storage disease due to acid maltase deficiency, infantile onset
- glycogen storage disease due to acid maltase deficiency, late-onset
- glycogen storage disease due to aldolase A deficiency
- glycogen storage disease due to glucose-6-phosphatase deficiency type IA
- glycogen storage disease due to glycogen branching enzyme deficiency
- glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form
- glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
- glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form
- glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form
- glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form
- glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form
- glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form
- glycogen storage disease due to lactate dehydrogenase H-subunit deficiency
- glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
- glycogen storage disease due to lactate dehydrogenase deficiency
- glycogen storage disease due to liver phosphorylase kinase deficiency
- glycogen storage disease due to muscle and heart glycogen synthase deficiency
- glycogen storage disease due to muscle beta-enolase deficiency
- glycogen storage disease due to phosphoglycerate kinase 1 deficiency
- glycogen storage disease due to phosphoglycerate mutase deficiency
- glycogen storage disease type 1 due to SLC37A4 mutation
