All diseases

OMIM ID
259900
OMIM term:
HYPEROXALURIA, PRIMARY, TYPE I; HP1
Alternative terms:
OXALOSIS I
GLYCOLIC ACIDURIA
ALANINE-GLYOXYLATE AMINOTRANSFERASE DEFICIENCY
PEROXISOMAL ALANINE:GLYOXYLATE AMINOTRANSFERASE DEFICIENCY
HEPATIC AGT DEFICIENCY
SERINE:PYRUVATE AMINOTRANSFERASE DEFICIENCY
(∗) Location:
2q37.3  
(†) Associated OMIM genes:
AGXT  
(‡) Associated MGI genes:
Agxt  

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