All diseases

OMIM ID
260000
OMIM term:
HYPEROXALURIA, PRIMARY, TYPE II
Alternative terms:
HP2
OXALOSIS II
GLYCERIC ACIDURIA
GLYOXYLATE REDUCTASE/HYDROXYPYRUVATE REDUCTASE DEFICIENCY
D-GLYCERATE DEHYDROGENASE DEFICIENCY
(∗) Location:
9p13.2  
(†) Associated OMIM genes:
GRHPR  
(‡) Associated MGI genes:
Grhpr  

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