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primary hyperoxaluria

Disease Summary
Associated Targets (18)
Tbio

11

Tchem

4

Tclin

3


Mondo Description A hereditary disorder characterized by excessive oxalate production, leading to hyperoxaluria.
Mondo Term and Equivalent IDs
MONDO:0002474:  primary hyperoxaluria
MESH:D006960: 
NCIT:C123158: 
OMIMPS:259900: 
Orphanet:416: 
SCTID:17901006: 
UMLS:C0020501: