(Q10376433)

English

Kelley–Seegmiller syndrome

human disease

Hypoxanthine guanine phosphoribosyltransferase partial deficiency
Kelley-Seegmiller syndrome
HRPT-related hyperuricemia

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No description defined

Statements

class of disease

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hypoxanthine-guanine phosphoribosyltransferase deficiency

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1 reference

Disease Ontology

24 November 2020

Disease Ontology ID

X-linked recessive disease

1 reference

Disease Ontology

24 November 2020

Disease Ontology ID

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discoverer or inventor

J. Edwin Seegmiller

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http://purl.obolibrary.org/obo/DOID_0112127

1 reference

Disease Ontology

24 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0112127

1 reference

Identifiers.org

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

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

24 November 2020

Disease Ontology ID

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Sitelinks

Wikipedia(3 entries)

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Wiktionary(0 entries)

Multilingual sites(0 entries)

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