primary hyperoxaluria
0 sources
Summary
primary hyperoxaluria is a rare disease[1]. It draws 161 Wikipedia views per month (rare disease category, ranking #221 of 627).[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: hyperoxaluria[4], carbohydrate metabolic disorder[5], kidney disease[6], disorder of glyoxylate metabolism[7]
- NCI Thesaurus ID: C123158[8]
- Health specialty: obstetrics and gynaecology[9], urology[10], medical genetics[11], endocrinology[12]
- Drug or therapy used for treatment: nedosiran[13]
- Genetic association: HOGA1[14]
- Exact match: http://purl.obolibrary.org/obo/DOID_2977[15], http://identifiers.org/doid/DOID:2977[16], http://purl.obolibrary.org/obo/HP_0003159[17]
- On focus list of Wikimedia project: WikiProject Medicine[18]
Why It Matters
primary hyperoxaluria is known by 6 alternative names across languages and contexts.[19]