(Q7243137)

English

primary hyperoxaluria

human disease

Hyperoxaluria, Primary

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Statements

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carbohydrate metabolic disorder

1 reference

30 November 2020

1 reference

15 May 2019

disorder of glyoxylate metabolism

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image

Structure of oxalate.svg
1,100 × 779; 2 KB

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health specialty

obstetrics and gynaecology

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urology

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medical genetics

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endocrinology

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drug or therapy used for treatment

nedosiran

1 reference

retrieved

13 November 2023

reference URL

https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/215842s000lbl.pdf

genetic association

HOGA1

1 reference

stated in

Mutations in DHDPSL Are Responsible For Primary Hyperoxaluria Type III

on focus list of Wikimedia project

WikiProject Medicine

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NCI Thesaurus ID

C123158

1 reference

15 May 2019

http://purl.obolibrary.org/obo/DOID_2977

1 reference

30 November 2020

http://identifiers.org/doid/DOID:2977

1 reference

stated in

Identifiers.org

reference URL

https://registry.identifiers.org/registry/doid

http://purl.obolibrary.org/obo/HP_0003159

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0003159

Identifiers

MeSH descriptor ID

D006960

subject named as

Hyperoxaluria, Primary

1 reference

15 May 2019

0 references

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C12.050.351.968.419.313.500

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C12.200.777.419.313.500

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C12.950.419.313.500

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PatientsLikeMe condition ID

primary-hyperoxaluria

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1 reference

30 November 2020

1 reference

imported from Wikimedia project

English Wikipedia

Genetics Home Reference Conditions ID

primary-hyperoxaluria

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1 reference

15 May 2019

JSTOR topic ID (archived)

primary-hyperoxaluria

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Microsoft Academic ID

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1 reference

15 May 2019

1 reference

15 May 2019

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

0 references

2 references

15 May 2019

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

1 reference

15 May 2019

Primary hyperoxaluria

0 references

(Q7243137)

primary hyperoxaluria

Statements

Identifiers

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Wikipedia(5 entries)

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