(Q54320724)
English
primary hyperoxaluria type I
human disease
- oxalosis I
- gylcolytic aciduria
- serine:pyruvate aminotransferase deficiency
- HP1
- Alanine-Glyoxylate Aminotransferase Deficiency
- Peroxisomal alanine-glyoxylate aminotransferase deficiency
- Glycolic aciduria
- Peroxisomal Alanine:Glyoxylate Aminotransferase Deficiency
- Oxalosis 1
- Serine pyruvate aminotransferase deficiency
- Primary Hyperoxaluria Type I
- Hepatic Agt Deficiency
- HYPEROXALURIA, PRIMARY, TYPE I; HP1
- Peroxisomal alanine glyoxylate aminotransferase deficiency
- HYPEROXALURIA, PRIMARY, TYPE I
- primary hyperoxaluria type 1
Statements
1 reference
1 reference
2 references
271.8
1 reference
C123212
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference