primary hyperoxaluria (Q7243137)

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Human disease

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Language	Label	Description	Also known as
English	primary hyperoxaluria	Human disease

Statements

instance of

rare disease

0 references

class of disease

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subclass of

hyperoxaluria

0 references

carbohydrate metabolic disorder

1 reference

stated in

Disease Ontology

retrieved

30 November 2020

Disease Ontology ID

DOID:2977

kidney disease

1 reference

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:2977

disorder of glyoxylate metabolism

0 references

image

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

0 references

health specialty

obstetrics and gynaecology

0 references

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

0 references

NCI Thesaurus ID

C123158

1 reference

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:2977

exact match

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

1 reference

stated in

Disease Ontology

retrieved

30 November 2020

Disease Ontology ID

DOID:2977

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

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:2977

MeSH tree code

C12.777.419.313.500

0 references

C13.351.968.419.313.500

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C16.320.565.202.460

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C18.452.648.202.460

0 references

PatientsLikeMe condition ID

primary-hyperoxaluria

0 references

KEGG ID

H00117

0 references

Disease Ontology ID

DOID:2977

1 reference

stated in

Disease Ontology

retrieved

30 November 2020

Disease Ontology ID

DOID:2977

DiseasesDB

6280

1 reference

imported from Wikimedia project

English Wikipedia

Genetics Home Reference Conditions ID

primary-hyperoxaluria

0 references

ICD-10-CM

E72.53

1 reference

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:2977

JSTOR topic ID

primary-hyperoxaluria

0 references

Microsoft Academic ID

2781092957

0 references

2909832588

0 references

OMIM ID

260000

1 reference

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:2977

613616

1 reference

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:2977

OpenAlex ID

C2781092957

1 reference

stated in

OpenAlex

retrieved

26 January 2022

reference URL

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

Orphanet ID

416

0 references

UMLS CUI

C0020500

2 references

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:2977

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0003159

C0020501

1 reference

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:2977

WikiProjectMed ID

Primary hyperoxaluria

0 references

 

Sitelinks

Wikipedia(5 entries)

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• bswiki Primarna hiperoksalurija
• enwiki Primary hyperoxaluria
• eswiki Hiperoxaluria primaria tipo 1
• frwiki Hyperoxalurie type 1
• mkwiki Примарна хипероксалурија

Wikibooks(0 entries)

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Wikinews(0 entries)

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Wikiquote(0 entries)

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Wikisource(0 entries)

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Wikiversity(0 entries)

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Wikivoyage(0 entries)

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Wiktionary(0 entries)

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Multilingual sites(0 entries)

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Retrieved from "https://www.wikidata.org/w/index.php?title=Q7243137&oldid=2092871572"