Orphanet: Primary hyperoxaluria type 1

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ORPHA:93598

Classification level: Subtype of disorder

Synonym(s):
- Glycolic aciduria
- Peroxisomal alanine-glyoxylate aminotransferase deficiency
Prevalence: -
Inheritance: Autosomal recessive
Age of onset: All ages
ICD-10: E74.8
OMIM: 259900
UMLS: C0268164
MeSH: C536414
GARD: 2835
MedDRA: -

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Primary hyperoxaluria type 1

ORPHA:93598

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