Mondo Disease Ontology
1483 terms(s) returned
| Term Type: | Record: 1201 to 1250 of 1483 Records | Page: 25 of 30, First Previous Next Last | Show Records Per Page |
- glycogen storage disease VII
- 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 disease, AGL-related, dog
- glycogen storage disease, G6PC1-related, dog
- glycogen storage disease, GAA-related, cattle
- glycogen storage disease, GAA-related, dog
- glycogen storage disease, GAA-related, domestic cat
- glycogen storage disease, PFKM-related, dog
- glycogen storage disease, PYGM-related, cattle
- glycogen storage disease, PYGM-related, sheep
- glycogen storage disease, non-human animal
- glycogen storage disease, ring-tailed coati
- glycogen storage disorder due to hepatic glycogen synthase deficiency
- glycogen synthase activity, transferring glucose-1-phosphate
- glycogen-rich carcinoma
- glycogen-rich clear cell breast carcinoma
- glycol
- glycolipid
- glycolipid biosynthetic process
- glycolipid metabolic process
- glycolysis from storage polysaccharide through glucose-1-phosphate
- glycolytic process
- glycolytic process through fructose-6-phosphate
- glycolytic process through glucose-1-phosphate
- glycolytic process through glucose-6-phosphate
- glycoprotein
- glycoprotein biosynthetic process
- glycoprotein complex
