Experimental Factor Ontology
2350 terms(s) returned
| Term Type: | Record: 1951 to 2000 of 2350 Records | Page: 40 of 47, First Previous Next Last | Show Records Per Page |
- 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
- glycogen storage disorder due to hepatic glycogen synthase deficiency
- glycogen synthase kinase-3 alpha/beta measurement
- glycogen synthase kinase-3 beta
- glycogenin-2
- glycohyocholate
- glycohyocholate measurement
- glycolipid transfer protein
- glycolipid transfer protein domain-containing protein 2
- glycolipid transfer protein domain-containing protein 2 measurement
- glycolipid transfer protein measurement
- glycolipid transfer protein, initiator methionine removed form
- glycolithocholate
- glycolithocholate measurement
- glycolithocholate sulfate measurement
- glycolytic process
- glycophorin
- glycophorin-A
- glycophorin-A measurement
- glycophorin-A, signal peptide removed form
- glycoprotein
- glycoprotein Xg
- glycoprotein Xg measurement
- glycoprotein biosynthetic process
- glycoprotein change measurement
- glycoprotein endo-alpha-1,2-mannosidase
- glycoprotein endo-alpha-1,2-mannosidase measurement
