Disease association ontology term - MONDO:0002474 - primary hyperoxaluria

Term summary

ID

MONDO:0002474

Name

primary hyperoxaluria

Ontology or CV name

Disease association

Definition

A hereditary disorder characterized by excessive oxalate production, leading to hyperoxaluria.

Parents

• excluded_subClassOf kidney disorder
• excluded_subClassOf disorder of glyoxylate metabolism
• excluded_subClassOf obsolete nephropathy secondary to a storage or other metabolic disease (obsolete MONDO:0019743)
• is_a inborn carbohydrate metabolic disorder

Annotation