(Q10295763)

English

hyperlysinemia

amino acid metabolic disorder that involves an abnormal increase of lysine in the blood

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Statements

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disorder of lysine and hydroxylysine metabolism

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amino acid metabolic disorder

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30 November 2020

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Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia

on focus list of Wikimedia project

WikiProject Medicine

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NCI Thesaurus ID

C123433

1 reference

15 May 2019

http://purl.obolibrary.org/obo/DOID_9274

1 reference

30 November 2020

http://identifiers.org/doid/DOID:9274

1 reference

stated in

Identifiers.org

reference URL

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

http://purl.obolibrary.org/obo/HP_0002161

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0002161

http://www.orpha.net/ORDO/Orphanet_2203

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Identifiers

2 references

15 May 2019

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0002161

MeSH tree code

C10.228.140.163.100.380

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1 reference

30 November 2020

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imported from Wikimedia project

English Wikipedia

Wikimedia import URL

https://en.wikipedia.org/w/index.php?title=Hyperlysinemia&oldid=892722208

1 reference

15 May 2019

Genetics Home Reference Conditions ID

hyperlysinemia

0 references

Human Phenotype Ontology ID

HP:0002161

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

1 reference

15 May 2019

1 reference

imported from Wikimedia project

English Wikipedia

Microsoft Academic ID

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1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

2 references

15 May 2019

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0002161

C0936256

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata

25 May 2023

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(Q10295763)

hyperlysinemia

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