Mondo Disease Ontology
1477 terms(s) returned
| Term Type: | Record: 1151 to 1200 of 1477 Records | Page: 24 of 30, First Previous Next Last | Show Records Per Page |
- glyceraldehyde-3-phosphate dehydrogenase [NAD(P)+] (phosphorylating) activity
- glyceraldehyde-3-phosphate dehydrogenase deficiency
- glycerol ether biosynthetic process
- glycerol ether metabolic process
- glycerol kinase activity
- glycerol kinase deficiency, adult form
- glycerol kinase deficiency, infantile form
- glycerol kinase deficiency, juvenile form
- glycerol metabolic process
- glycerol metabolism disease
- glycerolipid biosynthetic process
- glycerolipid metabolic process
- glyceronephosphate O-acyltransferase deficiency
- glycerophospholipid biosynthetic process
- glycerophospholipid metabolic process
- glycine N-methyltransferase deficiency
- glycine amidinotransferase activity
- glycine encephalopathy
- glycine encephalopathy 1
- glycine encephalopathy 2
- glycine metabolic process
- glycine metabolism disease
- glycogen biosynthetic process
- glycogen catabolic process
- glycogen metabolic process
- glycogen storage disease I
- glycogen storage disease II
- glycogen storage disease II, Japanese quail
- glycogen storage disease II, sheep
- glycogen storage disease III
- glycogen storage disease IV, dog
- glycogen storage disease IV, domestic cat
- glycogen storage disease IV, horse
- glycogen storage disease IX
- glycogen storage disease IXa1
- glycogen storage disease IXa2
- glycogen storage disease IXb
- glycogen storage disease IXc
- glycogen storage disease IXd
- glycogen storage disease Ib
- glycogen storage disease Id
- glycogen storage disease V
- glycogen storage disease VI
- 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
