primary hyperoxaluria
human disease
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primary hyperoxaluria
Summary
primary hyperoxaluria is a rare disease[1].
Key Facts
- primary hyperoxaluria's instance of is recorded as rare disease[2].
- primary hyperoxaluria's instance of is recorded as class of disease[3].
- primary hyperoxaluria is a type of hyperoxaluria[4].
- primary hyperoxaluria is a type of carbohydrate metabolic disorder[5].
- primary hyperoxaluria is a type of kidney disease[6].
- primary hyperoxaluria is a type of disorder of glyoxylate metabolism[7].
- primary hyperoxaluria's NCI Thesaurus ID is recorded as C123158[8].
- primary hyperoxaluria's health specialty is recorded as obstetrics and gynaecology[9].
- primary hyperoxaluria's health specialty is recorded as urology[10].
- primary hyperoxaluria's health specialty is recorded as medical genetics[11].
- primary hyperoxaluria's health specialty is recorded as endocrinology[12].
- primary hyperoxaluria's drug or therapy used for treatment is recorded as nedosiran[13].
- primary hyperoxaluria's genetic association is recorded as HOGA1[14].
- primary hyperoxaluria's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2977[15].
- primary hyperoxaluria's exact match is recorded as http://identifiers.org/doid/DOID:2977[16].
- primary hyperoxaluria's exact match is recorded as http://purl.obolibrary.org/obo/HP_0003159[17].
- primary hyperoxaluria's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].