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Hydroxyacyl glutathione hydrolase deficiency

MedGen UID:
481287
Concept ID:
C3279657
Disease or Syndrome
Synonym: GLYOXALASE II DEFICIENCY
 
Gene (location): HAGH (16p13.3)
 
Monarch Initiative: MONDO:0013535
OMIM®: 614033

Clinical features

From HPO
Glyoxalase deficiency
MedGen UID:
481288
Concept ID:
C3279658
Finding

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