primary hyperoxaluria type I (Q54320724)
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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
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | primary hyperoxaluria type I |
human disease |
|
Statements
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271.8
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C123212
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Identifiers
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